ATORVASTATIN CALCIUM- atorvastatin calcium tablet, film coated

United States - English - NLM (National Library of Medicine)

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Active ingredient:
ATORVASTATIN CALCIUM TRIHYDRATE (UNII: 48A5M73Z4Q) (ATORVASTATIN - UNII:A0JWA85V8F)
Available from:
Bryant Ranch Prepack
Administration route:
ORAL
Prescription type:
PRESCRIPTION DRUG
Therapeutic indications:
Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Drug therapy is recommended as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been inadequate. In patients with CHD or multiple risk factors for CHD, atorvastatin calcium tablets can be started simultaneously with diet. In adult patients without clinically evident coronary heart disease, but with multiple risk factors for coronary heart disease such as age, smoking, hypertension, low HDL-C, or a family history of early coronary heart disease, atorvastatin calcium tablets are indicated to: - Reduce the risk of myocardial infarction - Reduce the risk of stroke - Reduce the risk for revascularization procedures and angina In adult patients with type 2 diabetes, and without clinically evident coronary heart disease
Product summary:
Product: 63629-4796 Product: 63629-8032 NDC: 63629-8032-1 30 TABLET, FILM COATED in a BOTTLE NDC: 63629-8032-2 90 TABLET, FILM COATED in a BOTTLE
Authorization status:
Abbreviated New Drug Application
Authorization number:
63629-4796-1, 63629-4796-2, 63629-4796-3, 63629-4796-4, 63629-4796-5, 63629-8032-1, 63629-8032-2

ATORVASTATIN CALCIUM- atorvastatin calcium tablet, film coated

Bryant Ranch Prepack

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HIGHLIGHTS OF PRESCRIBING INFORMATION

These highlights do not include all the information needed to use ATORVASTATIN CALCIUM TABLETS

safely and effectively. See full prescribing information for ATORVASTATIN CALCIUM TABLETS.

ATORVASTATIN CALCIUM tablets, for oral use

Initial U.S. Approval: 1996

RECENT MAJOR CHANGES

Dosage and Administration, Dosage in Patients Taking Cyclosporine, Clarithromycin, Itraconazole, or Certain Protease

Inhibitors (2.6) 4/2019

Warnings and Precautions, Skeletal Muscle (5.1) 4/2019

INDICATIONS AND USAGE

Atorvastatin calcium tablets are a HMG-CoA reductase inhibitor indicated as an adjunct therapy to diet to:

Reduce the risk of MI, stroke, revascularization procedures, and angina in adult patients without CHD, but with multiple

risk factors (1.1).

Reduce the risk of MI and stroke in adult patients with type 2 diabetes without CHD, but with multiple risk factors (1.1).

Reduce the risk of non-fatal MI, fatal and non-fatal stroke, revascularization procedures, hospitalization for CHF, and

angina in adult patients with CHD (1.1).

Reduce elevated total-C, LDL-C, apo B, and TG levels and increase HDL-C in adult patients with primary hyperlipidemia

(heterozygous familial and nonfamilial) and mixed dyslipidemia (1.2).

Reduce elevated TG in adult patients with hypertriglyceridemia and primary dysbetalipoproteinemia (1.2).

Reduce total-C and LDL-C in patients with homozygous familial hypercholesterolemia (HoFH) (1.2).

Reduce elevated total-C, LDL-C, and apo B levels in pediatric patients, 10 years to 17 years of age, with heterozygous

familial hypercholesterolemia (HeFH) after failing an adequate trial of diet therapy (1.2).

Limitations of Use:

Atorvastatin calcium has not been studied in Fredrickson Types I and V dyslipidemias (1.3).

DOSAGE AND ADMINISTRATION

Dose range: 10 to 80 mg once daily (2.1).

Recommended start dose: 10 or 20 mg once daily (2.1).

Patients requiring large LDL-C reduction (>45%) may start at 40 mg once daily (2.1).

Pediatric patients with HeFH: starting dose: 10 mg once daily; dose range: 10 to 20 mg/day for patients 10 years to 17

years of age (2.2).

DOSAGE FORMS AND STRENGTHS

Tablets: 10 mg, 20 mg, 40 mg, and 80 mg of atorvastatin (3).

CONTRAINDICATIONS

Active liver disease, which may include unexplained persistent elevations in hepatic transaminase levels (4).

Hypersensitivity to any component of this medication (4).

Pregnancy (4, 8.1, 8.3).

Lactation (4, 8.2).

WARNINGS AND PRECAUTIONS

Skeletal muscle effects (e.g., myopathy and rhabdomyolysis): Risks increase when higher doses are used

concomitantly with cyclosporine and strong CYP3A4 inhibitors (e.g., clarithromycin, itraconazole, human

immunodeficiency virus (HIV) or hepatitis C virus (HCV) protease inhibitors). Predisposing factors include advanced

age (> 65), uncontrolled hypothyroidism, and renal impairment. Rare cases of rhabdomyolysis with acute renal failure

secondary to myoglobinuria have been reported. Advise patients to promptly report to their physician unexplained

and/or persistent muscle pain, tenderness, or weakness. Atorvastatin calcium therapy should be discontinued if

myopathy is diagnosed or suspected (2.6, 5.1, 8.5).

Liver enzyme abnormalities: Persistent elevations in hepatic transaminases can occur. Check liver enzyme tests before

initiating therapy and as clinically indicated thereafter (5.2).

A higher incidence of hemorrhagic stroke was seen in patients without CHD but with stroke or TIA within the previous 6

months in the atorvastatin calcium 80 mg group vs. placebo (5.5).

ADVERSE REACTIONS

The most commonly reported adverse reactions (incidence ≥ 2%) in patients treated with atorvastatin in placebo-

controlled trials regardless of causality were: nasopharyngitis, arthralgia, diarrhea, pain in extremity, and urinary tract

infection (6.1).

To report SUSPECTED ADVERSE REACTIONS, contact Apotex Corp. at 1-800-706-5575 or FDA at 1-800-FDA-

1088 or www.fda.gov/medwatch.

DRUG INTERACTIONS

Drug Interactions Associated with Increased Risk of Myopathy/Rhabdomyolysis (2.6, 5.1, 7, 12.3)

Interacting Agents

Pre scribing

Re comme ndations

Cyclosporine, tipranavir plus ritonavir, glecaprevir plus pibrentasvir

Avoid atorvastatin

Clarithromycin, itraconazole, saquinavir plus ritonavir, darunavir plus ritonavir,

fosamprenavir, fosamprenavir plus ritonavir, elbasvir plus grazoprevir.

Do not exceed 20 mg

atorvastatin daily

Ne lfinavir

Do not exceed 40 mg

atorvastatin daily

Lopinavir plus ritonavir, simeprevir, fibric acid derivatives, erythromycin, azole antifungals,

lipid-modifying doses of niacin, colchicine

Use with caution and lowest

dose necessary

Other Lipid-Lowering Medications: Use with fibrate products or lipid-modifying doses (≥1 g/day) of niacin increases the

risk of adverse skeletal muscle effects. Caution should be used when prescribing with atorvastatin (7).

Digoxin: Patients should be monitored appropriately (7.9).

Oral Contraceptives: Values for norethindrone and ethinyl estradiol may be increased (7.10).

Rifampin should be simultaneously co-administered with atorvastatin (7.8).

USE IN SPECIFIC POPULATIONS

Hepatic impairment: Plasma concentrations markedly increased in patients with chronic alcoholic liver disease (8.6,

12.3).

Females of reproductive potential: Advise females of reproductive potential to use effective contraception during

treatment with atorvastatin (8.3)

See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.

Revised: 8/2019

FULL PRESCRIBING INFORMATION: CONTENTS*

1 INDICATIONS AND USAGE

1.1 Prevention of Cardiovascular Disease in Adults

1.2 Hyperlipidemia

1.3 Limitations of Use

2 DOSAGE AND ADMINISTRATION

2.1 Hyperlipidemia and Mixed Dyslipidemia

2.2 Heterozygous Familial Hypercholesterolemia in Pediatric Patients (10 Years to 17 Years of

Age)

2.3 Homozygous Familial Hypercholesterolemia

2.4 Concomitant Lipid-Lowering Therapy

2.5 Dosage in Patients with Renal Impairment

2.6 Dosage in Patients Taking Cyclosporine, Clarithromycin, Itraconazole, or Certain Protease

Inhibitors

3 DOSAGE FORMS AND STRENGTHS

4 CONTRAINDICATIONS

5 WARNINGS AND PRECAUTIONS

5.1 Skeletal Muscle

5.2 Liver Dysfunction

5.2 Liver Dysfunction

5.3 Endocrine Function

5.4 CNS Toxicity

5.5 Use in Patients with Recent Stroke or TIA

6 ADVERSE REACTIONS

6.1 Clinical Trials Experience

6.2 Postmarketing Experience

7 DRUG INTERACTIONS

7.1 Strong Inhibitors of CYP 3A4

7.2 Grapefruit Juice

7.3 Cyclosporine

7.4 Glecaprevir and Pibrentasvir; Elbasvir and Grazoprevir

7.5 Gemfibrozil

7.6 Other Fibrates

7.7 Niacin

7.8 Rifampin or other Inducers of Cytochrome P450 3A4

7.9 Digoxin

7.10 Oral Contraceptives

7.11 Warfarin

7.12 Colchicine

8 USE IN SPECIFIC POPULATIONS

8.1 Pregnancy

8.2 Lactation

8.3 Females and Males of Reproductive Potential

8.4 Pediatric Use

8.5 Geriatric Use

8.6 Hepatic Impairment

10 OVERDOSAGE

11 DESCRIPTION

12 CLINICAL PHARMACOLOGY

12.1 Mechanism of Action

12.2 Pharmacodynamics

12.3 Pharmacokinetics

13 NONCLINICAL TOXICOLOGY

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

14 CLINICAL STUDIES

14.1 Prevention of Cardiovascular Disease

14.2 Hyperlipidemia and Mixed Dyslipidemia

14.3 Hypertriglyceridemia

14.4 Dysbetalipoproteinemia

14.5 Homozygous Familial Hypercholesterolemia

14.6 Heterozygous Familial Hypercholesterolemia in Pediatric Patients

16 HOW SUPPLIED/STORAGE AND HANDLING

17 PATIENT COUNSELING INFORMATION

17.1 Muscle Pain

17.2 Liver Enzymes

17.3 Embryofetal Toxicity

17.4 Lactation

FULL PRESCRIBING INFORMATION

Sections or subsections omitted from the full prescribing information are not listed.

1 INDICATIONS AND USAGE

Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in

individuals at significantly increased risk for atherosclerotic vascular disease due to

hypercholesterolemia. Drug therapy is recommended as an adjunct to diet when the response to a diet

restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been

inadequate. In patients with CHD or multiple risk factors for CHD, atorvastatin calcium tablets can be

started simultaneously with diet.

1.1 Prevention of Cardiovascular Disease in Adults

In adult patients without clinically evident coronary heart disease, but with multiple risk factors for

coronary heart disease such as age, smoking, hypertension, low HDL-C, or a family history of early

coronary heart disease, atorvastatin calcium tablets are indicated to:

Reduce the risk of myocardial infarction

Reduce the risk of stroke

Reduce the risk for revascularization procedures and angina

In adult patients with type 2 diabetes, and without clinically evident coronary heart disease, but with

multiple risk factors for coronary heart disease such as retinopathy, albuminuria, smoking, or

hypertension, atorvastatin calcium tablets are indicated to:

Reduce the risk of myocardial infarction

Reduce the risk of stroke

In adult patients with clinically evident coronary heart disease, atorvastatin calcium tablets are indicated

Reduce the risk of non-fatal myocardial infarction

Reduce the risk of fatal and non-fatal stroke

Reduce the risk for revascularization procedures

Reduce the risk of hospitalization for CHF

Reduce the risk of angina

1.2 Hyperlipidemia

Atorvastatin calcium tablets are indicated

As an adjunct to diet to reduce elevated total-C, LDL-C, apo B, and TG levels and to increase HDL-

C in adult patients with primary hypercholesterolemia (heterozygous familial and nonfamilial) and

mixed dyslipidemia (Fredrickson Types IIa and IIb);

As an adjunct to diet for the treatment of adult patients with elevated serum TG levels (Fredrickson

Type IV);

For the treatment of adult patients with primary dysbetalipoproteinemia (Fredrickson Type III) who

do not respond adequately to diet;

To reduce total-C and LDL-C in patients with homozygous familial hypercholesterolemia (HoFH)

as an adjunct to other lipid-lowering treatments (e.g., LDL apheresis) or if such treatments are

unavailable;

As an adjunct to diet to reduce total-C, LDL-C, and apo B levels in pediatric patients, 10 years to 17

years of age, with heterozygous familial hypercholesterolemia (HeFH) if after an adequate trial of

diet therapy the following findings are present:

a. LDL-C remains ≥ 190 mg/dL or

b. LDL-C remains ≥ 160 mg/dL and:

there is a positive family history of premature cardiovascular disease or

two or more other CVD risk factors are present in the pediatric patient

1.3 Limitations of Use

Atorvastatin calcium tablets have not been studied in conditions where the major lipoprotein abnormality

is elevation of chylomicrons (Fredrickson Types I and V).

2 DOSAGE AND ADMINISTRATION

2.1 Hyperlipidemia and Mixed Dyslipidemia

The recommended starting dose of atorvastatin calcium tablets are 10 or 20 mg once daily. Patients who

require a large reduction in LDL-C (more than 45%) may be started at 40 mg once daily. The dosage

range of atorvastatin calcium tablets are 10 to 80 mg once daily. Atorvastatin calcium tablets can be

administered as a single dose at any time of the day, with or without food. The starting dose and

maintenance doses of atorvastatin calcium tablets should be individualized according to patient

characteristics such as goal of therapy and response. After initiation and/or upon titration of atorvastatin

calcium tablets, lipid levels should be analyzed within 2 to 4 weeks and dosage adjusted accordingly.

2.2 Heterozygous Familial Hypercholesterolemia in Pediatric Patients (10 Years to 17 Years of

Age)

The recommended starting dose of atorvastatin calcium tablets is 10 mg/day; the usual dose range is 10

to 20 mg orally once daily [see Clinical Studies (14.6)]. Doses should be individualized according to the

recommended goal of therapy [see Indications and Usage (1.2) and Clinical Pharmacology (12)].

Adjustments should be made at intervals of 4 weeks or more.

2.3 Homozygous Familial Hypercholesterolemia

The dosage of atorvastatin calcium tablets in patients with HoFH is 10 to 80 mg daily. Atorvastatin

calcium tablets should be used as an adjunct to other lipid-lowering treatments (e.g., LDL apheresis) in

these patients or if such treatments are unavailable.

2.4 Concomitant Lipid-Lowering Therapy

Atorvastatin calcium tablets may be used with bile acid resins. The combination of HMG-CoA

reductase inhibitors (statins) and fibrates should generally be used with caution [see Warnings and

Precautions (5.1) and Drug Interactions (7)].

2.5 Dosage in Patients with Renal Impairment

Renal disease does not affect the plasma concentrations nor LDL-C reduction of atorvastatin; thus,

dosage adjustment in patients with renal dysfunction is not necessary [see Warnings and Precautions (5.1)

and Clinical Pharmacology (12.3)].

2.6 Dosage in Patients Taking Cyclosporine, Clarithromycin, Itraconazole, or Certain Protease

Inhibitors

In patients taking cyclosporine or the HIV protease inhibitor tipranavir plus ritonavir or the hepatitis C

virus (HCV) protease inhibitor glecaprevir plus pibrentasvir, therapy with atorvastatin calcium tablets

should be avoided. In patients with HIV taking lopinavir plus ritonavir, use the lowest dose necessary of

atorvastatin calcium tablets. In patients taking clarithromycin, itraconazole, elbasvir plus grazoprevir, or

in patients with HIV taking a combination of saquinavirplus ritonavir, darunavirplus ritonavir,

fosamprenavir, or fosamprenavir plus ritonavir, therapy with atorvastatin calcium tablets should be

limited to 20 mg, and appropriate clinical assessment is recommended to ensure that the lowest dose

necessary of atorvastatin calcium tablets is used. In patients taking the HIV protease inhibitor nelfinavir

therapy with atorvastatin calcium tablets should be limited to 40 mg. When co-prescribing atorvastatin

with other protease inhibitors, appropriate clinical assessment is recommended to ensure that the lowest

dose necessary of atorvastatin calcium tablets is used [see Warnings and Precautions (5.1) and Drug

Interactions (7)].

3 DOSAGE FORMS AND STRENGTHS

White to off-white, oval, biconvex, film-coated tablets containing 10, 20, 40, and 80 mg atorvastatin

calcium.

4 CONTRAINDICATIONS

Active Liver Disease, Which May Include Unexplained Persistent Elevations in Hepatic

Transaminase Levels

Hypersensitivity to Any Component of This Medication

Pregnancy [see Use in Specific Populations (8.1)].

Lactation [see Use in Specific Populations (8.2)].

5 WARNINGS AND PRECAUTIONS

5.1 Skeletal Muscle

Rare cases of rhabdomyolysis with acute renal failure secondary to myoglobinuria have been

reported with atorvastatin and with other drugs in this class. A history of renal impairment may be a

risk factor for the development of rhabdomyolysis. Such patients merit closer monitoring for skeletal

muscle effects.

Atorvastatin, like other statins, occasionally causes myopathy, defined as muscle aches or muscle

weakness in conjunction with increases in creatine phosphokinase (CPK) values >10 times ULN. The

concomitant use of higher doses of atorvastatin with certain drugs such as cyclosporine and strong

cytochrome P450 3A4 (CYP3A4) inhibitors (e.g. clarithromycin, itraconazole, and HIV and HCV

protease inhibitors) increases the risk of myopathy/rhabdomyolysis.

There have been rare reports of immune-mediated necrotizing myopathy (IMNM), an autoimmune

myopathy, associated with statin use. IMNM is characterized by: proximal muscle weakness and

elevated serum creatine kinase, which persist despite discontinuation of statin treatment; muscle biopsy

showing necrotizing myopathy without significant inflammation; improvement with immunosuppressive

agents.

Myopathy should be considered in any patient with diffuse myalgias, muscle tenderness or weakness,

and/or marked elevation of CPK. Patients should be advised to report promptly unexplained muscle pain,

tenderness, or weakness, particularly if accompanied by malaise or fever or if muscle signs and

symptoms persist after discontinuing atorvastatin. Atorvastatin therapy should be discontinued if

markedly elevated CPK levels occur or myopathy is diagnosed or suspected.

The risk of myopathy during treatment with drugs in this class is increased with concurrent

administration of the drugs listed in Table2. Physicians considering combined therapy of atorvastatin

with any of these drugs should carefully weigh the potential benefits and risks and should carefully

monitor patients for any signs or symptoms of muscle pain, tenderness, or weakness, particularly during

the initial months of therapy and during any periods of upward dosage titration of either drug. Lower

starting and maintenance doses of atorvastatin should be considered when taken concomitantly with the

aforementioned drugs [see Drug Interactions (7)]. Periodic creatine phosphokinase (CPK)

determinations may be considered in such situations, but there is no assurance that such monitoring will

prevent the occurrence of severe myopathy.

Prescribing recommendations for interacting agents are summarized in Table 2 [see Dosage and

Administration (2.6), Drug Interactions (7), and Clinical Pharmacology (12.3)].

Table 2. Drug Interactions Associated with Increased Risk of Myopathy/Rhabdomyolysis

Interacting Agents

Prescribing

Recommendations

Cyclosporine, tipranavir plus ritonavir, glecaprevir plus pibrentasvir

Avoid atorvastatin

Clarithromycin, itraconazole, saquinavir plus ritonavir*, darunavir plus

ritonavir, fosamprenavir, fosamprenavir plus ritonavir elbasvir plus

grazoprevir

Do not exceed 20 mg

atorvastatin daily

Nelfinavir

Do not exceed 40 mg

atorvastatin daily

Lopinavir plus ritonavir, simeprevir, fibric acid derivatives, erythromycin,

azole antifungals, lipid-modifying doses of niacin, colchicine

Use with caution and

lowest dose necessary

*Use the lowest dose necessary (12.3)

Atorvastatin therapy should be temporarily withheld or discontinued in any patient with an acute,

serious condition suggestive of a myopathy or having a risk factor predisposing to the

development of renal failure secondary to rhabdomyolysis (e.g., severe acute infection,

hypotension, major surgery, trauma, severe metabolic, endocrine and electrolyte disorders, and

uncontrolled seizures).

5.2 Liver Dysfunction

Statins, like some other lipid-lowering therapies, have been associated with biochemical abnormalities

of liver function. Persistent elevations (>3 times the upper limit of normal [ULN] occurring on 2

or more occasions) in serum transaminases occurred in 0.7% of patients who received

atorvastatin in clinical trials. The incidence of these abnormalities was 0.2%, 0.2%, 0.6%, and

2.3% for 10, 20, 40, and 80 mg, respectively.

One patient in clinical trials developed jaundice. Increases in liver function tests (LFT) in other patients

were not associated with jaundice or other clinical signs or symptoms. Upon dose reduction, drug

interruption, or discontinuation, transaminase levels returned to or near pretreatment levels without

sequelae. Eighteen of 30 patients with persistent LFT elevations continued treatment with a reduced

dose of atorvastatin.

It is recommended that liver enzyme tests be obtained prior to initiating therapy with atorvastatin and

repeated as clinically indicated. There have been rare postmarketing reports of fatal and non-fatal

hepatic failure in patients taking statins, including atorvastatin. If serious liver injury with clinical

symptoms and/or hyperbilirubinemia or jaundice occurs during treatment with atorvastatin, promptly

interrupt therapy. If an alternate etiology is not found, do not restart atorvastatin.

Atorvastatin should be used with caution in patients who consume substantial quantities of alcohol

and/or have a history of liver disease. Active liver disease or unexplained persistent transaminase

elevations are contraindications to the use of atorvastatin [see Contraindications (4)].

5.3 Endocrine Function

Increases in HbA1c and fasting serum glucose levels have been reported with HMG-CoA reductase

inhibitors, including atorvastatin.

Statins interfere with cholesterol synthesis and theoretically might blunt adrenal and/or gonadal steroid

production. Clinical studies have shown that atorvastatin does not reduce basal plasma cortisol

concentration or impair adrenal reserve. The effects of statins on male fertility have not been studied in

adequate numbers of patients. The effects, if any, on the pituitary-gonadal axis in premenopausal women

are unknown. Caution should be exercised if a statin is administered concomitantly with drugs that may

decrease the levels or activity of endogenous steroid hormones, such as ketoconazole, spironolactone,

and cimetidine.

5.4 CNS Toxicity

Brain hemorrhage was seen in a female dog treated for 3 months at 120 mg/kg/day. Brain hemorrhage

and optic nerve vacuolation were seen in another female dog that was sacrificed in moribund condition

after 11 weeks of escalating doses up to 280 mg/kg/day. The 120 mg/kg dose resulted in a systemic

exposure approximately 16 times the human plasma area-under-the-curve (AUC, 0 to 24 hours) based on

the maximum human dose of 80 mg/day. A single tonic convulsion was seen in each of 2 male dogs (one

treated at 10 mg/kg/day and one at 120 mg/kg/day) in a 2-year study. No CNS lesions have been

observed in mice after chronic treatment for up to 2 years at doses up to 400 mg/kg/day or in rats at

doses up to 100 mg/kg/day. These doses were 6 to 11 times (mouse) and 8 to 16 times (rat) the human

AUC (0 to 24) based on the maximum recommended human dose of 80 mg/day.

CNS vascular lesions, characterized by perivascular hemorrhages, edema, and mononuclear cell

infiltration of perivascular spaces, have been observed in dogs treated with other members of this class.

A chemically similar drug in this class produced optic nerve degeneration (Wallerian degeneration of

retinogeniculate fibers) in clinically normal dogs in a dose-dependent fashion at a dose that produced

plasma drug levels about 30 times higher than the mean drug level in humans taking the highest

recommended dose.

5.5 Use in Patients with Recent Stroke or TIA

In a post-hoc analysis of the Stroke Prevention by Aggressive Reduction in Cholesterol Levels

(SPARCL) study where atorvastatin calcium 80 mg vs. placebo was administered in 4,731 subjects

without CHD who had a stroke or TIA within the preceding 6 months, a higher incidence of

hemorrhagic stroke was seen in the atorvastatin calcium 80 mg group compared to placebo (55, 2.3%

atorvastatin vs. 33, 1.4% placebo; HR: 1.68, 95% CI: 1.09, 2.59; p=0.0168). The incidence of fatal

hemorrhagic stroke was similar across treatment groups (17 vs. 18 for the atorvastatin and placebo

groups, respectively). The incidence of nonfatal hemorrhagic stroke was significantly higher in the

atorvastatin group (38, 1.6%) as compared to the placebo group (16, 0.7%). Some baseline

characteristics, including hemorrhagic and lacunar stroke on study entry, were associated with a higher

incidence of hemorrhagic stroke in the atorvastatin group [see Adverse Reactions (6.1)].

6 ADVERSE REACTIONS

The following serious adverse reactions are discussed in greater detail in other sections of the label:

Rhabdomyolysis and myopathy [see Warnings and Precautions (5.1)]

Liver enzyme abnormalities [see Warnings and Precautions (5.2)]

6.1 Clinical Trials Experience

Because clinical trials are conducted under widely varying conditions, the adverse reaction rates

observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of

another drug and may not reflect the rates observed in clinical practice.

In the atorvastatin calcium placebo-controlled clinical trial database of 16,066 patients (8755

atorvastatin calcium vs. 7311 placebo; age range 10 to 93 years, 39% women, 91% Caucasians, 3%

Blacks, 2% Asians, 4% other) with a median treatment duration of 53 weeks, 9.7% of patients on

atorvastatin calcium and 9.5% of the patients on placebo discontinued due to adverse reactions

regardless of causality. The five most common adverse reactions in patients treated with atorvastatin

calcium that led to treatment discontinuation and occurred at a rate greater than placebo were: myalgia

(0.7%), diarrhea (0.5%), nausea (0.4%), alanine aminotransferase increase (0.4%), and hepatic enzyme

increase (0.4%).

The most commonly reported adverse reactions (incidence ≥ 2% and greater than placebo) regardless

of causality, in patients treated with atorvastatin calcium in placebo controlled trials (n=8755) were:

nasopharyngitis (8.3%), arthralgia (6.9%), diarrhea (6.8%), pain in extremity (6.0%), and urinary tract

nasopharyngitis (8.3%), arthralgia (6.9%), diarrhea (6.8%), pain in extremity (6.0%), and urinary tract

infection (5.7%).

Table 3 summarizes the frequency of clinical adverse reactions, regardless of causality, reported in ≥

2% and at a rate greater than placebo in patients treated with atorvastatin calcium (n=8755), from

seventeen placebo-controlled trials.

Table 3. Clinical adverse reactions occurring in ≥ 2% in patients treated with any dose of

atorvastatin calcium and at an incidence greater than placebo regardless of causality (% of

patients ).

Advers e

Any dose

10 mg

20 mg

40 mg

80 mg

Placebo

Reaction

N=8755

N=3908

N=188

N=604

N=4055

N=7311

Nasopharyngitis

12.9

Arthralgia

11.7

10.6

Diarrhea

14.1

Pain in extremity

Urinary tract

infection

Dyspepsia

Nausea

Musculoskeletal pain

Muscle Spasms

Myalgia

Insomnia

Pharyngolaryngeal

pain

Other adverse reactions reported in placebo-controlled studies include

Body as a whole: malaise, pyrexia; Digestive system: abdominal discomfort, eructation, flatulence,

hepatitis, cholestasis; Musculoskeletal system: musculoskeletal pain, muscle fatigue, neck pain, joint

swelling; Metabolic and nutritional system: transaminases increase, liver function test abnormal, blood

alkaline phosphatase increase, creatine phosphokinase increase, hyperglycemia; Nervous system:

nightmare; Respiratory system: epistaxis; Skin and appendages: urticaria; Special senses: vision blurred,

tinnitus; Urogenital system: white blood cells urine positive.

Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT)

In ASCOT [see Clinical Studies (14.1)] involving 10,305 participants (age range 40 to 80 years, 19%

women; 94.6% Caucasians, 2.6% Africans, 1.5% South Asians, 1.3% mixed/other) treated with

atorvastatin calcium 10 mg daily (n=5,168) or placebo (n=5,137), the safety and tolerability profile of

the group treated with atorvastatin calcium was comparable to that of the group treated with placebo

during a median of 3.3 years of follow-up.

Collaborative Atorvastatin Diabetes Study (CARDS)

In CARDS [see Clinical Studies (14.1)] involving 2,838 subjects (age range 39 to 77 years, 32% women;

94.3% Caucasians, 2.4% South Asians, 2.3% Afro-Caribbean, 1.0% other) with type 2 diabetes treated

with atorvastatin calcium 10 mg daily (n=1,428) or placebo (n=1,410), there was no difference in the

overall frequency of adverse reactions or serious adverse reactions between the treatment groups

during a median follow-up of 3.9 years. No cases of rhabdomyolysis were reported.

Treating to New Targets Study (TNT)

In TNT [see Clinical Studies (14.1)] involving 10,001 subjects (age range 29 to 78 years, 19% women;

*

Adverse Reaction ≥ 2% in any dose greater than placebo

94.1% Caucasians, 2.9% Blacks, 1.0% Asians, 2.0% other) with clinically evident CHD treated with

atorvastatin calcium 10 mg daily (n=5006) or atorvastatin calcium 80 mg daily (n=4995), there were

more serious adverse reactions and discontinuations due to adverse reactions in the high-dose

atorvastatin group (92, 1.8%; 497, 9.9%, respectively) as compared to the low-dose group (69, 1.4%;

404, 8.1%, respectively) during a median follow-up of 4.9 years. Persistent transaminase elevations (≥3

x ULN twice within 4 to 10 days) occurred in 62 (1.3%) individuals with atorvastatin 80 mg and in nine

(0.2%) individuals with atorvastatin 10 mg. Elevations of CK (≥ 10 x ULN) were low overall, but were

higher in the high-dose atorvastatin treatment group (13, 0.3%) compared to the low-dose atorvastatin

group (6, 0.1%).

Incremental Decrease in Endpoints through Aggressive Lipid Lowering Study (IDEAL)

In IDEAL [see Clinical Studies (14.1)] involving 8,888 subjects (age range 26 to 80 years, 19% women;

99.3% Caucasians, 0.4% Asians, 0.3% Blacks, 0.04% other) treated with atorvastatin calcium 80

mg/day (n=4439) or simvastatin 20 to 40 mg daily (n=4449), there was no difference in the overall

frequency of adverse reactions or serious adverse reactions between the treatment groups during a

median follow-up of 4.8 years.

Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL)

In SPARCL involving 4731 subjects (age range 21 to 92 years, 40% women; 93.3% Caucasians, 3.0%

Blacks, 0.6% Asians, 3.1% other) without clinically evident CHD but with a stroke or transient ischemic

attack (TIA) within the previous 6 months treated with atorvastatin calcium 80 mg (n=2365) or placebo

(n=2366) for a median follow-up of 4.9 years, there was a higher incidence of persistent hepatic

transaminase elevations (≥ 3 x ULN twice within 4 to 10 days) in the atorvastatin group (0.9%)

compared to placebo (0.1%). Elevations of CK (>10 x ULN) were rare, but were higher in the

atorvastatin group (0.1%) compared to placebo (0.0%). Diabetes was reported as an adverse reaction in

144 subjects (6.1%) in the atorvastatin group and 89 subjects (3.8%) in the placebo group [see Warnings

and Precautions (5.5)].

In a post-hoc analysis, atorvastatin calcium 80 mg reduced the incidence of ischemic stroke (218/2365,

9.2% vs. 274/2366, 11.6%) and increased the incidence of hemorrhagic stroke (55/2365, 2.3% vs.

33/2366, 1.4%) compared to placebo. The incidence of fatal hemorrhagic stroke was similar between

groups (17 atorvastatin calcium vs. 18 placebo). The incidence of non-fatal hemorrhagic strokes was

significantly greater in the atorvastatin group (38 non-fatal hemorrhagic strokes) as compared to the

placebo group (16 non-fatal hemorrhagic strokes). Subjects who entered the study with a hemorrhagic

stroke appeared to be at increased risk for hemorrhagic stroke [7 (16%) atorvastatin calcium vs. 2 (4%)

placebo].

There were no significant differences between the treatment groups for all-cause mortality: 216 (9.1%)

in the atorvastatin calcium 80 mg/day group vs. 211 (8.9%) in the placebo group. The proportions of

subjects who experienced cardiovascular death were numerically smaller in the atorvastatin calcium 80

mg group (3.3%) than in the placebo group (4.1%). The proportions of subjects who experienced non-

cardiovascular death were numerically larger in the atorvastatin calcium 80 mg group (5.0%) than in the

placebo group (4.0%).

Adverse Reactions from Clinical Studies of Atorvastatin Calcium in Pediatric Patients

In a 26-week controlled study in boys and postmenarchal girls with HeFH (ages 10 years to 17 years)

(n=140, 31% female; 92% Caucasians, 1.6% Blacks, 1.6% Asians, 4.8% other), the safety and

tolerability profile of atorvastatin calcium 10 to 20 mg daily, as an adjunct to diet to reduce total

cholesterol, LDL-C, and apo B levels, was generally similar to that of placebo [see Use in Special

Populations (8.4) and Clinical Studies (14.6)].

6.2 Postmarketing Experience

The following adverse reactions have been identified during postapproval use of atorvastatin calcium.

Because these reactions are reported voluntarily from a population of uncertain size, it is not always

possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Adverse reactions associated with atorvastatin calcium therapy reported since market introduction, that

are not listed above, regardless of causality assessment, include the following: anaphylaxis,

angioneurotic edema, bullous rashes (including erythema multiforme, Stevens-Johnson syndrome, and

toxic epidermal necrolysis), rhabdomyolysis, myositis, fatigue, tendon rupture, fatal and non-fatal

hepatic failure, dizziness, depression, peripheral neuropathy, pancreatitis and interstitial lung disease.

There have been rare reports of immune-mediated necrotizing myopathy associated with statin use [see

Warnings and Precautions (5.1)].

There have been rare postmarketing reports of cognitive impairment (e.g., memory loss, forgetfulness,

amnesia, memory impairment, confusion) associated with statin use. These cognitive issues have been

reported for all statins. The reports are generally nonserious, and reversible upon statin discontinuation,

with variable times to symptom onset (1 day to years) and symptom resolution (median of 3 weeks).

7 DRUG INTERACTIONS

The risk of myopathy during treatment with statins is increased with concurrent administration of fibric

acid derivatives, lipid-modifying doses of niacin, cyclosporine, or strong CYP 3A4 inhibitors (e.g.,

clarithromycin, HIV and HCV protease inhibitors, and itraconazole) [see Warnings and Precautions (5.1)

and Clinical Pharmacology (12.3)].

7.1 Strong Inhibitors of CYP 3A4

Atorvastatin is metabolized by cytochrome P450 3A4. Concomitant administration of atorvastatin with

strong inhibitors of CYP 3A4 can lead to increases in plasma concentrations of atorvastatin. The extent

of interaction and potentiation of effects depend on the variability of effect on CYP 3A4.

Clarithromycin

Atorvastatin AUC was significantly increased with concomitant administration of atorvastatin 80 mg

with clarithromycin (500 mg twice daily) compared to that of atorvastatin alone [see Clinical

Pharmacology (12.3)]. Therefore, in patients taking clarithromycin, caution should be used when the

atorvastatin dose exceeds 20 mg [see Dosage and Administration (2.6) and Warnings and Precautions

(5.1)].

Combination of Protease Inhibitors

Atorvastatin AUC was significantly increased with concomitant administration of atorvastatin with

several combinations of protease inhibitors [see Clinical Pharmacology (12.3)]. In patients taking

tipranavir plus ritonavir orglecaprevir plus pibrentasvir, concomitant use of atorvastatin should be

avoided. In patients taking lopinavir plus ritonavir, or simeprevir, use the lowest necessary atorvastatin

dose. In patients taking saquinavir plus ritonavir, darunavir plus ritonavir, fosamprenavir, fosamprenavir

plus ritonavir, or elbasvir plus grazoprevir, the dose of atorvastatin should not exceed 20 mg. In patients

taking nelfinavir the dose of atorvastatin should not exceed 40 mg and close clinical monitoring is

recommended [see Dosage and Administration (2.6) and Warnings and Precautions (5.1)].

Itraconazole

Atorvastatin AUC was significantly increased with concomitant administration of atorvastatin 40 mg and

itraconazole 200 mg [see Clinical Pharmacology (12.3)]. Therefore, in patients taking itraconazole,

caution should be used when the atorvastatin dose exceeds 20 mg [see Dosage and Administration (2.6)

and Warnings and Precautions (5.1)].

7.2 Grapefruit Juice

Contains one or more components that inhibit CYP 3A4 and can increase plasma concentrations of

atorvastatin, especially with excessive grapefruit juice consumption (>1.2 liters per day).

7.3 Cyclosporine

Atorvastatin is a substrate of the hepatic transporters. Atorvastatin-metabolites are substrates of the

OATP1B1 transporter. Inhibitors of the OATP1B1 (e.g., cyclosporine) can increase the bioavailability

of atorvastatin. Atorvastatin AUC was significantly increased with concomitant administration of

atorvastatin 10 mg and cyclosporine 5.2 mg/kg/day compared to that of atorvastatin alone [see Clinical

Pharmacology (12.3)]. The co-administration of atorvastatin with cyclosporine should be avoided [see

Warnings and Precautions (5.1)].

7.4 Glecaprevir and Pibrentasvir; Elbasvir and Grazoprevir

Concomitant administration of glecaprevir and pibrentasvir or elbasvir and grazoprevir may lead to

increased plasma concentrations of atorvastatin and an increased risk of myopathy.

Coadministration of glecaprevir and pibrentasvir with atorvastatin increase plasma concentrations of

atorvastatin by 8.3-fold due in part to BCRP, OATP1B1/1B3, and CYP3A inhibition; therefore,

coadministration of atorvastatin in patients receiving concomitant medications with products containing

glecaprevir and pibrentasvir is not recommended.

Coadministration of elbasvir and grazoprevir with atorvastatin increase plasma concentrations of

atorvastatin by 1.9-fold due in part to BCRP, OATP1B1/1B3, and CYP3A inhibition; therefore, the dose

of atorvastatin should not exceed 20 mg daily in patients receiving concomitant medications with

products containing elbasvir and grazoprevir [see Dosage and Administration (2.6), Warnings and

Precautions (5.1), and Clinical Pharmacology (12.3)]

7.5 Gemfibrozil

Due to an increased risk of myopathy/rhabdomyolysis when HMG-CoA reductase inhibitors are co-

administered with gemfibrozil, concomitant administration of atorvastatin with gemfibrozil should be

avoided [see Warnings and Precautions (5.1)].

7.6 Other Fibrates

Because it is known that the risk of myopathy during treatment with HMG-CoA reductase inhibitors is

increased with concurrent administration of other fibrates, atorvastatin should be administered with

caution when used concomitantly with other fibrates [see Warnings and Precautions (5.1)].

7.7 Niacin

The risk of skeletal muscle effects may be enhanced when atorvastatin is used in combination with

niacin; a reduction in atorvastatin dosage should be considered in this setting [see Warnings and

Precautions (5.1)].

7.8 Rifampin or other Inducers of Cytochrome P450 3A4

Concomitant administration of atorvastatin with inducers of cytochrome P450 3A4 (e.g., efavirenz,

rifampin) can lead to variable reductions in plasma concentrations of atorvastatin. Due to the dual

interaction mechanism of rifampin, simultaneous co-administration of atorvastatin with rifampin is

recommended, as delayed administration of atorvastatin after administration of rifampin has been

associated with a significant reduction in atorvastatin plasma concentrations.

7.9 Digoxin

When multiple doses of atorvastatin and digoxin were co-administered, steady state plasma digoxin

concentrations increased [see Clinical Pharmacology (12.3)]. Patients taking digoxin should be monitored

appropriately.

7.10 Oral Contraceptives

Co-administration of atorvastatin and an oral contraceptive increased AUC values for norethindrone and

ethinyl estradiol [see Clinical Pharmacology (12.3)]. These increases should be considered when

selecting an oral contraceptive for a woman taking atorvastatin.

7.11 Warfarin

Atorvastatin had no clinically significant effect on prothrombin time when administered to patients

receiving chronic warfarin treatment.

7.12 Colchicine

Cases of myopathy, including rhabdomyolysis, have been reported with atorvastatin co-administered

with colchicine, and caution should be exercised when prescribing atorvastatin with colchicine.

8 USE IN SPECIFIC POPULATIONS

8.1 Pregnancy

Risk Summary

Atorvastatin calcium is contraindicated for use in pregnant women since safety in pregnant women has

not been established and there is no apparent benefit of lipid lowering drugs during pregnancy. Because

HMG-CoA reductase inhibitors decrease cholesterol synthesis and possibly the synthesis of other

biologically active substances derived from cholesterol, atorvastatin calcium may cause fetal harm

when administered to a pregnant woman. Atorvastatin calcium should be discontinued as soon as

pregnancy is recognized [see Contraindications (4)]. Limited published data on the use of atorvastatin are

insufficient to determine a drug-associated risk of major congenital malformations or miscarriage. In

animal reproduction studies in rats and rabbits there was no evidence of embryo-fetal toxicity or

congenital malformations at doses up to 30 and 20 times, respectively, the human exposure at the

maximum recommended human dose (MRHD) of 80 mg, based on body surface area (mg/m ). In rats

administered atorvastatin during gestation and lactation, decreased postnatal growth and development

was observed at doses ≥ 6 times the MRHD (see Data).

The estimated background risk of major birth defects and miscarriage for the indicated population is

unknown. In the U.S. general population, the estimated background risk of major birth defects and

miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.

Data

Human Data

Limited published data on atorvastatin calcium from observational studies, meta-analyses and case

reports have not shown an increased risk of major congenital malformations or miscarriage. Rare

reports of congenital anomalies have been received following intrauterine exposure to other HMG-

CoA reductase inhibitors. In a review of approximately 100 prospectively followed pregnancies in

women exposed to simvastatin or lovastatin, the incidences of congenital anomalies, spontaneous

abortions, and fetal deaths/stillbirths did not exceed what would be expected in the general population.

The number of cases is adequate to exclude a ≥3 to 4-fold increase in congenital anomalies over the

background incidence. In 89% of the prospectively followed pregnancies, drug treatment was initiated

prior to pregnancy and was discontinued at some point in the first trimester when pregnancy was

identified.

Animal Data

Atorvastatin crosses the rat placenta and reaches a level in fetal liver equivalent to that of maternal

plasma. Atorvastatin was administered to pregnant rats and rabbits during organogenesis at oral doses up

to 300 mg/kg/day and 100 mg/kg/day, respectively. Atorvastatin was not teratogenic in rats at doses up

to 300 mg/kg/day or in rabbits at doses up to 100 mg/kg/day. These doses resulted in multiples of about

30 times (rat) or 20 times (rabbit) the human exposure at the MRHD based on surface area (mg/m ). In

rats, the maternally toxic dose of 300 mg/kg resulted in increased post-implantation loss and decreased

fetal body weight. At the maternally toxic doses of 50 and 100 mg/kg/day in rabbits, there was increased

post-implantation loss, and at 100 mg/kg/day fetal body weights were decreased.

In a study in pregnant rats administered 20, 100, or 225 mg/kg/day from gestation day 7 through to

lactation day 20 (weaning), there was decreased survival at birth, postnatal day 4, weaning, and post-

weaning in pups of mothers dosed with 225 mg/kg/day, a dose at which maternal toxicity was observed.

Pup body weight was decreased through postnatal day 21 at 100 mg/kg/day, and through postnatal day 91

at 225 mg/kg/day. Pup development was delayed (rotorod performance at 100 mg/kg/day and acoustic

startle at 225 mg/kg/day; pinnae detachment and eye-opening at 225 mg/kg/day). These doses correspond

to 6 times (100 mg/kg) and 22 times (225 mg/kg) the human exposure at the MRHD, based on AUC.

8.2 Lactation

Risk Summary

Atorvastatin calcium use is contraindicated during breastfeeding [see Contraindications (4)]. There is no

available information on the effects of the drug on the breastfed infant or the effects of the drug on milk

production. It is not known whether atorvastatin is present in human milk, but it has been shown that

another drug in this class passes into human milk and atorvastatin is present in rat milk. Because of the

potential for serious adverse reactions in a breastfed infant, advise women that breastfeeding is not

recommended during treatment with atorvastatin calcium.

8.3 Females and Males of Reproductive Potential

Contraception

Atorvastatin calcium may cause fetal harm when administered to a pregnant woman. Advise females of

reproductive potential to use effective contraception during treatment with atorvastatin calcium [see Use

in Specific Populations (8.1)].

8.4 Pediatric Use

Heterozygous Familial Hypercholesterolemia (HeFH) The safety and effectiveness of atorvastatin

calcium have been established in pediatric patients, 10 years to 17 years of age, with HeFH as an adjunct

to diet to reduce total cholesterol, LDL-C, and apo B levels when, after an adequate trial of diet

therapy, the following are present:

LDL-C ≥ 190 mg/dL, or

LDL-C ≥ 160 mg/dL and

a positive family history of FH, or premature CVD in a first, or second-degree relative, or

two or more other CVD risk factors are present.

Use of atorvastatin calcium for this indication is supported by evidence from [see Dosage and

Administration (2.2), Adverse Reactions (6.1), Clinical Pharmacology (12.3), and Clinical Studies (14.6)]:

A placebo-controlled clinical trial of 6 months duration in 187 boys and postmenarchal girls, 10

years to 17 years of age. Patients treated with 10 mg or 20 mg daily atorvastatin calcium had an

adverse reaction profile generally similar to that of patients treated with placebo. In this limited

controlled study, there was no significant effect on growth or sexual maturation in boys or on

menstrual cycle length in girls.

Advise postmenarchal girls of contraception recommendations, if appropriate for the patient [see Use in

Specific Populations (8.1), (8.3)].

The long-term efficacy of atorvastatin calcium therapy initiated in childhood to reduce morbidity and

mortality in adulthood has not been established.

The safety and efficacy of atorvastatin calcium have not been established in pediatric patients younger

than 10 years of age with HeFH.

Additional pediatric use information is approved for Pfizer’s LIPITOR (atorvastatin calcium) tablets.

However, due to Pfizer’s marketing exclusivity rights, this drug product is not labeled with that pediatric

information.

Homozygous Familial Hypercholesterolemia (HoFH) Clinical efficacy of atorvastatin calcium with

dosages up to 80 mg/day for 1 year was evaluated in an uncontrolled study of patients with HoFH

including 8 pediatric patients [see Clinical Studies (14.5)].

8.5 Geriatric Use

Of the 39,828 patients who received atorvastatin calcium in clinical studies, 15,813 (40%) were ≥65

years old and 2,800 (7%) were ≥75 years old. No overall differences in safety or effectiveness were

observed between these subjects and younger subjects, and other reported clinical experience has not

identified differences in responses between the elderly and younger patients, but greater sensitivity of

some older adults cannot be ruled out. Since advanced age (≥65 years) is a predisposing factor for

myopathy, atorvastatin calcium should be prescribed with caution in the elderly.

8.6 Hepatic Impairment

Atorvastatin calcium is contraindicated in patients with active liver disease which may include

unexplained persistent elevations in hepatic transaminase levels [see Contraindications (4) and Clinical

Pharmacology (12.3)].

10 OVERDOSAGE

There is no specific treatment for atorvastatin overdosage. In the event of an overdose, the patient

should be treated symptomatically, and supportive measures instituted as required. Due to extensive

drug binding to plasma proteins, hemodialysis is not expected to significantly enhance atorvastatin

clearance.

11 DESCRIPTION

Atorvastatin calcium is a synthetic lipid-lowering agent. Atorvastatin is an inhibitor of 3-hydroxy-3-

methylglutaryl-coenzyme A (HMG-CoA) reductase. This enzyme catalyzes the conversion of HMG-

CoA to mevalonate, an early and rate-limiting step in cholesterol biosynthesis.

The drug substance used in atorvastatin calcium tablets, USP is atorvastatin calcium in the form of

propylene glycol solvate. The chemical name for atorvastatin calcium propylene glycol solvate is

calcium bis((3R,5R)-7-[3-(anilinocarbonyl)-5-(4-fluorophenyl)-2-isopropyl-4-phenyl-1H-pyrrol-1-yl]-

3,5-dihydroxyheptanoate) propylene glycol solvate. The empirical formula of atorvastatin calcium

propylene glycol solvate is C

H CaF N O * C H O and its molecular weight is 1231.46 g/mol.

Its structural formula is:

Atorvastatin calcium is a white to off-white solid that is insoluble in aqueous solutions of pH 4 and

below. Atorvastatin calcium is slightly soluble in distilled water, pH 7.4 phosphate buffer, and

acetonitrile; slightly soluble in ethanol; and freely soluble in methanol.

Atorvastatin calcium tablets, USP for oral administration contain 10, 20, 40, or 80 mg atorvastatin and

the following inactive ingredients: calcium acetate, colloidal silicon dioxide, croscarmellose sodium,

hydroxypropyl cellulose, hypromellose, magnesium stearate (vegetable source), microcrystalline

cellulose, polyethylene glycol, sodium carbonate, and titanium dioxide.

12 CLINICAL PHARMACOLOGY

12.1 Mechanism of Action

Atorvastatin is a selective, competitive inhibitor of HMG-CoA reductase, the rate-limiting enzyme that

converts 3-hydroxy-3-methylglutaryl-coenzyme A to mevalonate, a precursor of sterols, including

cholesterol.

In animal models, atorvastatin calcium lowers plasma cholesterol and lipoprotein levels by inhibiting

HMG-CoA reductase and cholesterol synthesis in the liver and by increasing the number of hepatic

LDL receptors on the cell surface to enhance uptake and catabolism of LDL; atorvastatin calcium also

reduces LDL production and the number of LDL particles.

12.2 Pharmacodynamics

Atorvastatin, as well as some of its metabolites, are pharmacologically active in humans. The liver is

the primary site of action and the principal site of cholesterol synthesis and LDL clearance. Drug

dosage, rather than systemic drug concentration, correlates better with LDL-C reduction.

Individualization of drug dosage should be based on therapeutic response [see Dosage and

Administration (2)].

12.3 Pharmacokinetics

Absorption

Atorvastatin is rapidly absorbed after oral administration; maximum plasma concentrations occur within

1 to 2 hours. Extent of absorption increases in proportion to atorvastatin dose. The absolute

bioavailability of atorvastatin (parent drug) is approximately 14% and the systemic availability of HMG-

CoA reductase inhibitory activity is approximately 30%. The low systemic availability is attributed to

presystemic clearance in gastrointestinal mucosa and/or hepatic first-pass metabolism. Although food

decreases the rate and extent of drug absorption by approximately 25% and 9%, respectively, as

assessed by C

and AUC, LDL-C reduction is similar whether atorvastatin is given with or without

food. Plasma atorvastatin concentrations are lower (approximately 30% for C

and AUC) following

evening drug administration compared with morning. However, LDL-C reduction is the same regardless

of the time of day of drug administration [see Dosage and Administration (2)].

Distribution

Mean volume of distribution of atorvastatin is approximately 381 liters. Atorvastatin is ≥98% bound to

plasma proteins. A blood/plasma ratio of approximately 0.25 indicates poor drug penetration into red

blood cells. Based on observations in rats, atorvastatin is likely to be secreted in human milk [see

Contraindications (4) and Use in Specific Populations (8.2)].

Metabolism

Atorvastatin is extensively metabolized to ortho- and parahydroxylated derivatives and various beta-

oxidation products. In vitro inhibition of HMG-CoA reductase by ortho- and parahydroxylated

metabolites is equivalent to that of atorvastatin. Approximately 70% of circulating inhibitory activity for

HMG-CoA reductase is attributed to active metabolites. In vitro studies suggest the importance of

atorvastatin metabolism by cytochrome P450 3A4, consistent with increased plasma concentrations of

atorvastatin in humans following co-administration with erythromycin, a known inhibitor of this isozyme

[see Drug Interactions (7.1)]. In animals, the ortho-hydroxy metabolite undergoes further

glucuronidation.

Excretion

Atorvastatin and its metabolites are eliminated primarily in bile following hepatic and/or extra-hepatic

metabolism; however, the drug does not appear to undergo enterohepatic recirculation. Mean plasma

elimination half-life of atorvastatin in humans is approximately 14 hours, but the half-life of inhibitory

activity for HMG-CoA reductase is 20 to 30 hours due to the contribution of active metabolites. Less

than 2% of a dose of atorvastatin is recovered in urine following oral administration.

Specific Populations

Geriatric

Plasma concentrations of atorvastatin are higher (approximately 40% for C

and 30% for AUC) in

healthy elderly subjects (age ≥65 years) than in young adults. Clinical data suggest a greater degree of

LDL-lowering at any dose of drug in the elderly patient population compared to younger adults [see Use

in Specific Populations (8.5)].

Pediatric

Apparent oral clearance of atorvastatin in pediatric subjects appeared similar to that of adults when

scaled allometrically by body weight as the body weight was the only significant covariate in

atorvastatin population PK model with data including pediatric HeFH patients (ages 10 years to 17 years

of age, n=29) in an open-label, 8-week study.

Gender

Plasma concentrations of atorvastatin in women differ from those in men (approximately 20% higher for

and 10% lower for AUC); however, there is no clinically significant difference in LDL-C

reduction with atorvastatin between men and women.

Renal Impairment

Renal disease has no influence on the plasma concentrations or LDL-C reduction of atorvastatin; thus,

dose adjustment in patients with renal dysfunction is not necessary [see Dosage and Administration (2.5)

and Warnings and Precautions (5.1)].

Hemodialysis

While studies have not been conducted in patients with end-stage renal disease, hemodialysis is not

expected to significantly enhance clearance of atorvastatin since the drug is extensively bound to plasma

proteins.

Hepatic Impairment

In patients with chronic alcoholic liver disease, plasma concentrations of atorvastatin are markedly

increased. C

and AUC are each 4-fold greater in patients with Childs-Pugh A disease. C

AUC are approximately 16-fold and 11-fold increased, respectively, in patients with Childs-Pugh B

disease [see Contraindications (4)].

Drug Interaction Studies

Atorvastatin is a substrate of the hepatic transporters, OATP1B1 and OATP1B3 transporter. Metabolites

of atorvastatin are substrates of OATP1B1. Atorvastatin is also identified as a substrate of the efflux

transporter BCRP, which may limit the intestinal absorption and biliary clearance of atorvastatin.

TABLE 4. Effect of Co-administered Drugs on the Pharmacokinetics of Atorvastatin

Co-administered drug and dosing regimen

Atorvas tatin

Dose (mg)

Ratio of

AUC

Ratio of

C

Cyclosporine 5.2 mg/kg/day, stable dose

10 mg QD for 28

days

8.69

10.66

Tipranavir 500 mg BID /ritonavir 200 mg BID, 7

days

10 mg, SD

9.36

8.58

#Glecaprevir 400 mg QD / pibrentasvir 120 mg

QD , 7 days

10 mg QD for 7

days

8.28

22.00

Telaprevir 750 mg q8h, 10 days

20 mg, SD

7.88

10.60

Saquinavir 400 mg BID / ritonavir 400 mg BID ,

15 days

40 mg QD for 4

days

3.93

4.31

#Elbasvir 50 mg QD / grazoprevir 200 mg QD , 13

days

10 mg SD

1.94

4.34

#Simeprevir 150 mg QD , 10 days

40 mg SD

2.12

1.70

Clarithromycin 500 mg BID , 9 days

80 mg QD for 8

days

4.54

5.38

Darunavir 300 mg BID /ritonavir 100 mg BID , 9

days

10 mg QD for 4

days

3.45

2.25

Itraconazole 200 mg QD , 4 days

40 mg SD

3.32

1.20

Fosamprenavir 700 mg BID/ritonavir 100 mg BID ,

14 days

10 mg QD for 4

days

2.53

2.84

Fosamprenavir 1400 mg BID , 14 days

10 mg QD for 4

days

2.30

4.04

Nelfinavir 1250 mg BID , 14 days

10 mg QD for 28

days

1.74

2.22

Grapefruit Juice, 240 mL QD *

40 mg, SD

1.37

1.16

Diltiazem 240 mg QD , 28 days

40 mg, SD

1.51

1.00

Erythromycin 500 mg QID , 7 days

10 mg, SD

1.33

1.38

Amlodipine 10 mg, single dose

80 mg, SD

1.18

0.91

Cimetidine 300 mg QID , 2 weeks

10 mg QD for 2

weeks

1.00

0.89

Colestipol 10 mg BID , 24 weeks

40 mg QD for 8

weeks

0.74**

Maalox TC 30 mL QID, 17 days

10 mg QD for 15

days

0.66

0.67

Efavirenz 600 mg QD , 14 days

10 mg for 3 days

0.59

1.01

Rifampin 600 mg QD , 7 days (co-administered)

40 mg SD

1.12

2.90

Rifampin 600 mg QD , 5 days (doses separated)

40 mg SD

0.20

0.60

Gemfibrozil 600mg BID , 7 days

40mg SD

1.35

1.00

Fenofibrate 160mg QD , 7 days

40mg SD

1.03

1.02

Boceprevir 800 mg TID , 7 days

40 mg SD

2.32

2.66

Represents ratio of treatments (co-administered drug plus atorvastatin vs.atorvastatin alone).

See Sections 5.1 and 7 for clinical significance.

* Greater increases in AUC (ratio of AUC up to 2.5) and/or C

(ratio of C

up to 1.71) have been

reported with excessive grapefruit consumption (≥ 750 mL to 1.2 liters per day).

&

max

&

#, ‡

&

** Ratio based on a single sample taken 8 to 16 h post dose.

Due to the dual interaction mechanism of rifampin, simultaneous co-administration of atorvastatin with

rifampin is recommended, as delayed administration of atorvastatin after administration of rifampin has

been associated with a significant reduction in atorvastatin plasma concentrations.

The dose of saquinavir plus ritonavir in this study is not the clinically used dose. The increase in

atorvastatin exposure when used clinically is likely to be higher than what was observed in this study.

Therefore, caution should be applied and the lowest dose necessary should be used.

a Once daily

b Twice daily

c Single dose

d Three times daily

e Four times daily

f Every 8 hours

TABLE 5. Effect of Atorvastatin on the Pharmacokinetics of Co-administered Drugs

Atorvas tatin

Co-administered drug and dosing regimen

Drug/Dose (mg)

Ratio of

AUC

Ratio of

C

80 mg QD for

15 days

Antipyrine, 600 mg SD

1.03

0.89

80 mg QD for

10 days

Digoxin 0.25 mg QD , 20 days

1.15

1.20

40 mg QD for

22 days

Oral contraceptive QD , 2 months - norethindrone 1 mg -

ethinyl estradiol 35 mcg

1.28 1.19

1.23 1.30

10 mg, SD

Tipranavir 500 mg BID /ritonavir 200 mg BID , 7 days

1.08

0.96

10 mg QD for 4

days

Fosamprenavir 1400 mg BID , 14 days

0.73

0.82

10 mg QD for 4

days

Fosamprenavir 700 mg BID/ritonavir 100 mg BID , 14 days

0.99

0.94

See Section 7 for clinical significance.

a Once daily

b Twice daily

c Single dose

13 NONCLINICAL TOXICOLOGY

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

In a 2-year carcinogenicity study in rats at dose levels of 10, 30, and 100 mg/kg/day, 2 rare tumors were

found in muscle in high-dose females: in one, there was a rhabdomyosarcoma and, in another, there was

a fibrosarcoma. This dose represents a plasma AUC (0 to 24) value of approximately 16 times the mean

human plasma drug exposure after an 80 mg oral dose.

A 2-year carcinogenicity study in mice given 100, 200, or 400 mg/kg/day resulted in a significant

increase in liver adenomas in high-dose males and liver carcinomas in high-dose females. These

max

findings occurred at plasma AUC (0 to 24) values of approximately 6 times the mean human plasma drug

exposure after an 80 mg oral dose.

In vitro, atorvastatin was not mutagenic or clastogenic in the following tests with and without metabolic

activation: the Ames test with Salmonella typhimurium and Escherichia coli, the HGPRT forward mutation

assay in Chinese hamster lung cells, and the chromosomal aberration assay in Chinese hamster lung

cells. Atorvastatin was negative in the in vivo mouse micronucleus test.

In female rats, atorvastatin at doses up to 225 mg/kg (56 times the human exposure) did not cause adverse

effects on fertility. Studies in male rats performed at doses up to 175 mg/kg (15 times the human

exposure) produced no changes in fertility. There was aplasia and aspermia in the epididymis of 2 of 10

rats treated with 100 mg/kg/day of atorvastatin for 3 months (16 times the human AUC at the 80 mg

dose); testis weights were significantly lower at 30 and 100 mg/kg and epididymal weight was lower at

100 mg/kg. Male rats given 100 mg/kg/day for 11 weeks prior to mating had decreased sperm motility,

spermatid head concentration, and increased abnormal sperm. Atorvastatin caused no adverse effects on

semen parameters, or reproductive organ histopathology in dogs given doses of 10, 40, or 120 mg/kg

for two years.

14 CLINICAL STUDIES

14.1 Prevention of Cardiovascular Disease

In the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT), the effect of atorvastatin calcium on fatal

and non-fatal coronary heart disease was assessed in 10,305 hypertensive patients 40 to 80 years of age

(mean of 63 years), without a previous myocardial infarction and with TC levels ≤251 mg/dL (6.5

mmol/L). Additionally, all patients had at least 3 of the following cardiovascular risk factors: male

gender (81.1%), age >55 years (84.5%), smoking (33.2%), diabetes (24.3%), history of CHD in a first-

degree relative (26%), TC:HDL >6 (14.3%), peripheral vascular disease (5.1%), left ventricular

hypertrophy (14.4%), prior cerebrovascular event (9.8%), specific ECG abnormality (14.3%),

proteinuria/albuminuria (62.4%). In this double-blind, placebo-controlled study, patients were treated

with anti-hypertensive therapy (Goal BP <140/90 mm Hg for non-diabetic patients; <130/80 mm Hg for

diabetic patients) and allocated to either atorvastatin calcium 10 mg daily (n=5,168) or placebo

(n=5,137), using a covariate adaptive method which took into account the distribution of nine baseline

characteristics of patients already enrolled and minimized the imbalance of those characteristics across

the groups. Patients were followed for a median duration of 3.3 years.

The effect of 10 mg/day of atorvastatin calcium on lipid levels was similar to that seen in previous

clinical trials.

Atorvastatin calcium significantly reduced the rate of coronary events [either fatal coronary heart

disease (46 events in the placebo group vs. 40 events in the atorvastatin calcium group) or non-fatal MI

(108 events in the placebo group vs. 60 events in the atorvastatin calcium group)] with a relative risk

reduction of 36% [(based on incidences of 1.9% for atorvastatin calcium vs. 3.0% for placebo),

p=0.0005 (see Figure 1)]. The risk reduction was consistent regardless of age, smoking status, obesity,

or presence of renal dysfunction. The effect of atorvastatin calcium was seen regardless of baseline

LDL levels. Due to the small number of events, results for women were inconclusive.

Figure 1: Effect of Atorvastatin Calcium 10 mg/day on Cumulative Incidence of Non-Fatal

Myocardial Infarction or Coronary Heart Disease Death (in ASCOT-LLA)

Atorvastatin calcium also significantly decreased the relative risk for revascularization procedures by

42% (incidences of 1.4% for atorvastatin calcium and 2.5% for placebo). Although the reduction of

fatal and non-fatal strokes did not reach a pre-defined significance level (p=0.01), a favorable trend was

observed with a 26% relative risk reduction (incidences of 1.7% for atorvastatin calcium and 2.3% for

placebo). There was no significant difference between the treatment groups for death due to

cardiovascular causes (p=0.51) or noncardiovascular causes (p=0.17).

In the Collaborative Atorvastatin Diabetes Study (CARDS), the effect of atorvastatin calcium on

cardiovascular disease (CVD) endpoints was assessed in 2838 subjects (94% white, 68% male), ages

40 to 75 with type 2 diabetes based on WHO criteria, without prior history of cardiovascular disease

and with LDL ≤ 160 mg/dL and TG ≤ 600 mg/dL. In addition to diabetes, subjects had 1 or more of the

following risk factors: current smoking (23%), hypertension (80%), retinopathy (30%), or

microalbuminuria (9%) or macroalbuminuria (3%). No subjects on hemodialysis were enrolled in the

study. In this multicenter, placebo-controlled, double-blind clinical trial, subjects were randomly

allocated to either atorvastatin calcium 10 mg daily (1429) or placebo (1411) in a 1:1 ratio and were

followed for a median duration of 3.9 years. The primary endpoint was the occurrence of any of the

major cardiovascular events: myocardial infarction, acute CHD death, unstable angina, coronary

revascularization, or stroke. The primary analysis was the time to first occurrence of the primary

endpoint.

Baseline characteristics of subjects were: mean age of 62 years, mean HbA1c 7.7%; median LDL-C 120

mg/dL; median TC 207 mg/dL; median TG 151 mg/dL; median HDL-C 52 mg/dL.

The effect of atorvastatin calcium 10 mg/day on lipid levels was similar to that seen in previous clinical

trials.

Atorvastatin calcium significantly reduced the rate of major cardiovascular events (primary endpoint

events) (83 events in the atorvastatin calcium group vs. 127 events in the placebo group) with a relative

risk reduction of 37%, HR 0.63, 95% CI (0.48, 0.83) (p=0.001) (see Figure 2). An effect of atorvastatin

calcium was seen regardless of age, sex, or baseline lipid levels.

Atorvastatin calcium significantly reduced the risk of stroke by 48% (21 events in the atorvastatin

calcium group vs. 39 events in the placebo group), HR 0.52, 95% CI (0.31, 0.89) (p=0.016) and reduced

the risk of MI by 42% (38 events in the atorvastatin calcium group vs. 64 events in the placebo group),

HR 0.58, 95.1% CI (0.39, 0.86) (p=0.007). There was no significant difference between the treatment

groups for angina, revascularization procedures, and acute CHD death.

There were 61 deaths in the atorvastatin calcium group vs. 82 deaths in the placebo group (HR 0.73,

p=0.059).

Figure 2: Effect of Atorvastatin Calcium 10 mg/day on Time to Occurrence of Major

Cardiovascular Event (myocardial infarction, acute CHD death, unstable angina, coronary

revascularization, or stroke) in CARDS

In the Treating to New Targets Study (TNT), the effect of atorvastatin calcium 80 mg/day vs.

atorvastatin calcium 10 mg/day on the reduction in cardiovascular events was assessed in 10,001

subjects (94% white, 81% male, 38% ≥65 years) with clinically evident coronary heart disease who had

achieved a target LDL-C level <130 mg/dL after completing an 8-week, open-label, run-in period with

atorvastatin calcium 10 mg/day. Subjects were randomly assigned to either 10 mg/day or 80 mg/day of

atorvastatin calcium and followed for a median duration of 4.9 years. The primary endpoint was the

time-to-first occurrence of any of the following major cardiovascular events (MCVE): death due to

CHD, non-fatal myocardial infarction, resuscitated cardiac arrest, and fatal and non-fatal stroke. The

mean LDL-C, TC, TG, non-HDL, and HDL cholesterol levels at 12 weeks were 73, 145, 128, 98, and

47 mg/dL during treatment with 80 mg of atorvastatin calcium and 99, 177, 152, 129, and 48 mg/dL

during treatment with 10 mg of atorvastatin calcium.

Treatment with atorvastatin calcium 80 mg/day significantly reduced the rate of MCVE (434 events in

the 80 mg/day group vs. 548 events in the 10 mg/day group) with a relative risk reduction of 22%, HR

0.78, 95% CI (0.69, 0.89), p=0.0002 (see Figure 3 and Table 6). The overall risk reduction was

consistent regardless of age (<65, ≥65) or gender.

Figure 3: Effect of Atorvastatin Calcium 80 mg/day vs. 10 mg/day on Time to Occurrence of

Major Cardiovascular Events (TNT)

TABLE 6. Overview of Efficacy Results in TNT

Endpoint

Atorvas tatin

Atorvas tatin

10 mg

80 mg

HR (95%CI)

(N=5006)

(N=4995)

PRIMARY ENDPOINT

n

(%)

n

(%)

First major cardiovascular endpoint

(10.9)

(8.7)

0.78 (0.69, 0.89)

Components of the Primary Endpoint

CHD death

(2.5)

(2.0)

0.80 (0.61, 1.03)

Non-fatal, non-procedure related

(6.2)

(4.9)

0.78 (0.66, 0.93)

Resuscitated cardiac arrest

(0.5)

(0.5)

0.96 (0.56, 1.67)

Stroke (fatal and non-fatal)

(3.1)

(2.3)

0.75 (0.59, 0.96)

SECONDARY ENDPOINTS*

First CHF with hospitalization

(3.3)

(2.4)

0.74 (0.59, 0.94)

First PVD endpoint

(5.6)

(5.5)

0.97 (0.83, 1.15)

First CABG or other coronary

revascularization procedure

(18.1)

(13.4)

0.72 (0.65, 0.80)

First documented angina endpoint

(12.3)

(10.9)

0.88 (0.79, 0.99)

All-cause mortality

(5.6)

(5.7)

1.01 (0.85, 1.19)

Components of All-Cause Mortality

Cardiovascular death

(3.1)

(2.5)

0.81 (0.64, 1.03)

Noncardiovascular death

(2.5)

(3.2)

1.25 (0.99, 1.57)

Cancer death

(1.5)

(1.7)

1.13 (0.83, 1.55)

Other non-CV death

(0.9)

(1.2)

1.35 (0.91, 2.00)

Suicide, homicide, and other

traumatic non-CV death

(0.2)

(0.3)

1.67 (0.73, 3.82)

Atorvastatin 80 mg: atorvastatin 10 mg

Component of other secondary endpoints

* Secondary endpoints not included in primary endpoint

HR=hazard ratio; CHD=coronary heart disease; CI=confidence interval; MI=myocardial infarction;

CHF=congestive heart failure; CV=cardiovascular; PVD=peripheral vascular disease;

a

CABG=coronary artery bypass graft

Confidence intervals for the Secondary Endpoints were not adjusted for multiple comparisons

Of the events that comprised the primary efficacy endpoint, treatment with atorvastatin calcium 80

mg/day significantly reduced the rate of non-fatal, non-procedure related MI and fatal and non-fatal

stroke, but not CHD death or resuscitated cardiac arrest (Table 6). Of the predefined secondary

endpoints, treatment with atorvastatin calcium 80 mg/day significantly reduced the rate of coronary

revascularization, angina, and hospitalization for heart failure, but not peripheral vascular disease. The

reduction in the rate of CHF with hospitalization was only observed in the 8% of patients with a prior

history of CHF.

There was no significant difference between the treatment groups for all-cause mortality (Table 6). The

proportions of subjects who experienced cardiovascular death, including the components of CHD death

and fatal stroke, were numerically smaller in the atorvastatin calcium 80 mg group than in the atorvastatin

calcium 10 mg treatment group. The proportions of subjects who experienced noncardiovascular death

were numerically larger in the atorvastatin calcium 80 mg group than in the atorvastatin calcium 10 mg

treatment group.

In the Incremental Decrease in Endpoints Through Aggressive Lipid Lowering Study (IDEAL),

treatment with atorvastatin calcium 80 mg/day was compared to treatment with simvastatin 20 to 40

mg/day in 8,888 subjects up to 80 years of age with a history of CHD to assess whether reduction in

CV risk could be achieved. Patients were mainly male (81%), white (99%) with an average age of 61.7

years, and an average LDL-C of 121.5 mg/dL at randomization; 76% were on statin therapy. In this

prospective, randomized, open-label, blinded endpoint (PROBE) trial with no run-in period, subjects

were followed for a median duration of 4.8 years. The mean LDL-C, TC, TG, HDL, and non-HDL

cholesterol levels at Week 12 were 78, 145, 115, 45, and 100 mg/dL during treatment with 80 mg of

atorvastatin calcium and 105, 179, 142, 47, and 132 mg/dL during treatment with 20 to 40 mg of

simvastatin.

There was no significant difference between the treatment groups for the primary endpoint, the rate of

first major coronary event (fatal CHD, non-fatal MI, and resuscitated cardiac arrest): 411 (9.3%) in the

atorvastatin calcium 80 mg/day group vs. 463 (10.4%) in the simvastatin 20 to 40 mg/day group, HR

0.89, 95% CI ( 0.78, 1.01), p=0.07.

There were no significant differences between the treatment groups for all-cause mortality: 366 (8.2%)

in the atorvastatin calcium 80 mg/day group vs. 374 (8.4%) in the simvastatin 20 to 40 mg/day group.

The proportions of subjects who experienced CV or non-CV death were similar for the atorvastatin

calcium 80 mg group and the simvastatin 20 to 40 mg group.

14.2 Hyperlipidemia and Mixed Dyslipidemia

Atorvastatin calcium reduces total-C, LDL-C, VLDL-C, apo B, and TG, and increases HDL-C in

patients with hyperlipidemia (heterozygous familial and nonfamilial) and mixed dyslipidemia

(Fredrickson Types IIa and IIb). Therapeutic response is seen within 2 weeks, and maximum response is

usually achieved within 4 weeks and maintained during chronic therapy.

Atorvastatin calcium is effective in a wide variety of patient populations with hyperlipidemia, with and

without hypertriglyceridemia, in men and women, and in the elderly.

In two multicenter, placebo-controlled, dose-response studies in patients with hyperlipidemia,

atorvastatin calcium given as a single dose over 6 weeks, significantly reduced total-C, LDL-C, apo B,

and TG. (Pooled results are provided in Table 7.)

TABLE 7. Dose Response in Patients With Primary Hyperlipidemia (Adjusted Mean % Change

From Baseline)

Non-HDL-

*

Dose

LDL-C

Apo B

HDL-C

HDL-C

Placebo

In patients with Fredrickson Types IIa and IIb hyperlipoproteinemia pooled from 24 controlled trials, the

median (25

and 75

percentile) percent changes from baseline in HDL-C for atorvastatin calcium 10,

20, 40, and 80 mg were 6.4 (-1.4, 14), 8.7 (0, 17), 7.8 (0, 16), and 5.1 (-2.7, 15), respectively.

Additionally, analysis of the pooled data demonstrated consistent and significant decreases in total-C,

LDL-C, TG, total-C/HDL-C, and LDL-C/HDL-C.

In three multicenter, double-blind studies in patients with hyperlipidemia, atorvastatin calcium was

compared to other statins. After randomization, patients were treated for 16 weeks with either

atorvastatin calcium 10 mg per day or a fixed dose of the comparative agent (Table 8).

TABLE 8. Mean Percentage Change From Baseline at Endpoint (Double-Blind, Randomized,

Active-Controlled Trials)

Treatment

(Daily Dose)

Total-C

LDL-C

Apo B

HDL-C

Non-HDL-

HDL-C

Study 1

Atorvastatin 10 mg

Lovastatin 20 mg

95% CI for Diff

-9.2, -6.5

-10.7, -7.1 -10.0, -6.5 -15.2, -7.1

-1.7, 2.0

-11.1, -7.1

Study 2

Atorvastatin 10 mg

Pravastatin 20 mg

95% CI for Diff

-10.8, -6.1 -14.5, -8.2 -13.4, -7.4 -14.1, -0.7

-4.9, 1.6

-11.5, -4.1

Study 3

Atorvastatin 10 mg

Simvastatin 10 mg

95% CI for Diff

-8.7, -2.7

-10.1, -2.6

-8.0, -1.1

-15.1, -0.7

-4.3, 3.9

-9.6, -1.9

A negative value for the 95% CI for the difference between treatments favors atorvastatin for all

except HDL-C, for which a positive value favors atorvastatin. If the range does not include 0, this

indicates a statistically significant difference.

Significantly different from lovastatin, ANCOVA, p ≤0.05

Significantly different from pravastatin, ANCOVA, p ≤0.05

Significantly different from simvastatin, ANCOVA, p ≤0.05

The impact on clinical outcomes of the differences in lipid-altering effects between treatments shown in

Table 8 is not known. Table 8 does not contain data comparing the effects of atorvastatin 10 mg and

higher doses of lovastatin, pravastatin, and simvastatin. The drugs compared in the studies summarized

in the table are not necessarily interchangeable.

14.3 Hypertriglyceridemia

The response to atorvastatin calcium in 64 patients with isolated hypertriglyceridemia (Fredrickson

Results are pooled from 2 dose-response studies.

Type IV) treated across several clinical trials is shown in the table below (Table 9). For the atorvastatin

calcium -treated patients, median (min, max) baseline TG level was 565 (267 to 1502).

TABLE 9. Combined Patients With Isolated Elevated TG: Median (min,

max) Percentage Change From Baseline

Placebo

(N=12)

Atorvastatin

10 mg

(N=37)

Atorvastatin

20 mg

(N=13)

Atorvastatin

80 mg

(N=14)

T riglycerides

-12.4 (-36.6,

82.7)

-41.0 (-76.2,

49.4)

-38.7 (-62.7,

29.5)

-51.8 (-82.8,

41.3)

Total-C

-2.3 (-15.5,

24.4)

-28.2 (-44.9, -

6.8)

-34.9 (-49.6, -

15.2)

-44.4 (-63.5, -

3.8)

LDL-C

3.6 (-31.3,

31.6)

-26.5 (-57.7,

9.8)

-30.4 (-53.9,

0.3)

-40.5 (-60.6, -

13.8)

HDL-C

3.8 (-18.6,

13.4)

13.8 (-9.7,

61.5)

11.0 (-3.2,

25.2)

7.5 (-10.8,

37.2)

VLDL-C

-1.0 (-31.9,

53.2)

-48.8 (-85.8,

57.3)

-44.6 (-62.2, -

10.8)

-62.0 (-88.2,

37.6)

non-HDL-C

-2.8 (-17.6,

30.0)

-33.0 (-52.1, -

13.3)

-42.7 (-53.7, -

17.4)

-51.5 (-72.9, -

4.3)

14.4 Dysbetalipoproteinemia

The results of an open-label crossover study of 16 patients (genotypes: 14 apo E2/E2 and 2 apo E3/E2)

with dysbetalipoproteinemia (Fredrickson Type III) are shown in the table below (Table 10).

TABLE 10. Open-Label Crossover Study of 16 Patients

With Dysbetalipoproteinemia (Fredrickson Type III)

Median % Change (min, max)

Median

(min, max) at

Baseline

(mg/dL)

Atorvastatin

10 mg

Atorvastatin

80 mg

Total-C

442 (225,

1320)

-37 (-85, 17)

-58 (-90, -31)

T riglycerides

678 (273,

5990)

-39 (-92, -8)

-53 (-95, -30)

IDL-C + VLDL-

215 (111,

613)

-32 (-76, 9)

-63 (-90, -8)

non-HDL-C

411 (218,

1272)

-43 (-87, -19)

-64 (-92, -36)

14.5 Homozygous Familial Hypercholesterolemia

In a study without a concurrent control group, 29 patients ages 6 years to 37 years with HoFH received

maximum daily doses of 20 to 80 mg of atorvastatin calcium. The mean LDL-C reduction in this study

was 18%. Twenty-five patients with a reduction in LDL-C had a mean response of 20% (range of 7% to

53%, median of 24%); the remaining 4 patients had 7% to 24% increases in LDL-C. Five of the 29

patients had absent LDL-receptor function. Of these, 2 patients also had a portacaval shunt and had no

significant reduction in LDL-C. The remaining 3 receptor-negative patients had a mean LDL-C

reduction of 22%.

14.6 Heterozygous Familial Hypercholesterolemia in Pediatric Patients

In a double-blind, placebo-controlled study followed by an open-label phase, 187 boys and

postmenarchal girls 10 years to 17 years of age (mean age 14.1 years) with heterozygous familial

hypercholesterolemia (HeFH) or severe hypercholesterolemia, were randomized to atorvastatin

calcium (n=140) or placebo (n=47) for 26 weeks and then all received atorvastatin calcium for 26

weeks. Inclusion in the study required 1) a baseline LDL-C level ≥ 190 mg/dL or 2) a baseline LDL-C

level ≥ 160 mg/dL and positive family history of FH or documented premature cardiovascular disease

in a first or second-degree relative. The mean baseline LDL-C value was 218.6 mg/dL (range: 138.5 to

385.0 mg/dL) in the atorvastatin calcium group compared to 230.0 mg/dL (range: 160.0 to 324.5 mg/dL)

in the placebo group. The dosage of atorvastatin calcium (once daily) was 10 mg for the first 4 weeks

and uptitrated to 20 mg if the LDL-C level was > 130 mg/dL. The number of atorvastatin calcium-treated

patients who required uptitration to 20 mg after Week 4 during the double-blind phase was 78 (55.7%).

Atorvastatin calcium significantly decreased plasma levels of total-C, LDL-C, triglycerides, and

apolipoprotein B during the 26-week double-blind phase (see Table 11).

TABLE 11. Lipid-altering Effects of Atorvastatin Calcium in Adolescent Boys

and Girls with Heterozygous Familial Hypercholesterolemia or Severe

Hypercholesterolemia (Mean Percentage Change From Baseline at Endpoint

in Intention-to-Treat Population)

DOSAGE

Total-C

LDL-C

HDL-C

Apolipoprotein B

Placebo

-1.5

-0.4

-1.9

Atorvastatin

Calcium

Tablets

-31.4

-39.6

-12.0

-34.0

The mean achieved LDL-C value was 130.7 mg/dL (range: 70.0 to 242.0 mg/dL) in the atorvastatin

calcium group compared to 228.5 mg/dL (range: 152.0 to 385.0 mg/dL) in the placebo group during the

26-week double-blind phase.

The long-term efficacy of atorvastatin calcium therapy in childhood to reduce morbidity and mortality in

adulthood has not been established.

Additional pediatric use information is approved for Pfizer’s LIPITOR (atorvastatin calcium) tablets.

However, due to Pfizer’s marketing exclusivity rights, this drug product is not labeled with that pediatric

information.

16 HOW SUPPLIED/STORAGE AND HANDLING

Product: 63629-4796

Product: 63629-8032

NDC: 63629-8032-1 30 TABLET, FILM COATED in a BOTTLE

NDC: 63629-8032-2 90 TABLET, FILM COATED in a BOTTLE

17 PATIENT COUNSELING INFORMATION

Advise the patient to read the FDA-approved patient labeling (Patient Information).

Patients taking atorvastatin calcium tablets should be advised that cholesterol is a chronic condition and

they should adhere to their medication along with their National Cholesterol Education Program

(NCEP)-recommended diet, a regular exercise program as appropriate, and periodic testing of a fasting

lipid panel to determine goal attainment.

Patients should be advised about substances they should not take concomitantly with atorvastatin

[see Warnings and Precautions (5.1)]. Patients should also be advised to inform other healthcare

professionals prescribing a new medication that they are taking atorvastatin calcium tablets.

17.1 Muscle Pain

All patients starting therapy with atorvastatin calcium tablets should be advised of the risk of myopathy

and told to report promptly any unexplained muscle pain, tenderness, or weakness particularly if

accompanied by malaise or fever or if these muscle signs or symptoms persist after discontinuing

atorvastatin calcium. The risk of this occurring is increased when taking certain types of medication or

consuming larger quantities (>1 liter) of grapefruit juice. They should discuss all medication, both

prescription and over the counter, with their healthcare professional.

17.2 Liver Enzymes

It is recommended that liver enzyme tests be performed before the initiation of atorvastatin calcium

tablets and if signs or symptoms of liver injury occur. All patients treated with atorvastatin calcium

tablets should be advised to report promptly any symptoms that may indicate liver injury, including

fatigue, anorexia, right upper abdominal discomfort, dark urine, or jaundice.

17.3 Embryofetal Toxicity

Advise females of reproductive potential of the risk to a fetus, to use an effective contraception during

treatment and to inform their healthcare provider of a known or suspected pregnancy [see

Contraindications (4) and Use in Specific Populations (8.1, 8.3)].

17.4 Lactation

Advise women not to breastfeed during treatment with atorvastatin calcium tablets [see Contraindications

(4) and Use in Specific Populations (8.2)].

All registered trademarks in this document are the property of their respective owners.

APOTEX INC.

ATORVASTATIN CALCIUM TABLETS, USP

10 mg, 20 mg, 40 mg, and 80 mg

Manufactured By

Manufactured For

Apotex Inc.

Apotex Corp.

Toronto, Ontario

Weston, Florida

Canada, M9L 1T9

33326

Revised: May 2019

Rev. 16

Patient Information

Atorvastatin Calcium Tablets, USP

(a tor″ va stat′ in kal′ see um)

Read the Patient Information that comes with atorvastatin calcium tablets before you start taking it and

each time you get a refill. There may be new information. This leaflet does not take the place of talking

with your doctor about your condition or treatment.

If you have any questions about atorvastatin calcium tablets, ask your doctor or pharmacist.

What Are Atorvastatin Calcium Tablets?

Atorvastatin calcium tablets are a prescription medicine that lowers cholesterol in your blood. It lowers

the LDL-C ("bad" cholesterol) and triglycerides in your blood. It can raise your HDL-C ("good"

cholesterol) as well. Atorvastatin calcium tablets are for adults and children over 10 whose cholesterol

does not come down enough with exercise and a low-fat diet alone.

Atorvastatin calcium tablets can lower the risk for heart attack, stroke, certain types of heart surgery,

and chest pain in patients who have heart disease or risk factors for heart disease such as:

age, smoking, high blood pressure, low HDL-C, heart disease in the family.

Atorvastatin calcium tablets can lower the risk for heart attack or stroke in patients with diabetes and risk

factors such as:

eye problems, kidney problems, smoking, or high blood pressure.

Atorvastatin calcium tablets start to work in about 2 weeks.

What is Cholesterol?

Cholesterol and triglycerides are fats that are made in your body. They are also found in foods. You

need some cholesterol for good health, but too much is not good for you. Cholesterol and triglycerides

can clog your blood vessels. It is especially important to lower your cholesterol if you have heart

disease, smoke, have diabetes or high blood pressure, are older, or if heart disease starts early in your

family.

Who Should Not Take Atorvastatin Calcium Tablets?

Do not take atorvastatin calcium tablets if you:

are pregnant or think you may be pregnant, or are planning to become pregnant. Atorvastatin calcium

tablets may harm your unborn baby. If you get pregnant, stop taking atorvastatin calcium tablets and

call your doctor right away.

are breast feeding. Atorvastatin calcium can pass into your breast milk and may harm your baby.

have liver problems.

are allergic to atorvastatin calcium tablets or any of its ingredients. The active ingredient is

atorvastatin. See the end of this leaflet for a complete list of ingredients in atorvastatin calcium

tablets.

Atorvastatin calcium tablets dosing have not been established in children under 10 years of age.

Before You Start Atorvastatin Calcium Tablets

Tell your doctor if you:

have muscle aches or weakness

drink more than 2 glasses of alcohol daily

have diabetes

have a thyroid problem

have kidney problems

Some medicines should not be taken with atorvastatin calcium tablets. Tell your doctor about all the

medicines you take, including prescription and non-prescription medicines, vitamins, and herbal

supplements. Atorvastatin calcium tablets and certain other medicines can interact causing serious side

effects. Especially tell your doctor if you take medicines for:

your immune system

cholesterol

1

infections

birth control

heart failure

HIV or AIDS

hepatitis C virus

Know all the medicines you take. Keep a list of them with you to show your doctor and pharmacist.

How Should I Take Atorvastatin Calcium Tablets?

Take atorvastatin calcium tablets exactly as prescribed by your doctor. Do not change your dose or

stop atorvastatin calcium tablets without talking to your doctor. Your doctor may do blood tests to

check your cholesterol levels during your treatment with atorvastatin calcium tablets. Your dose of

atorvastatin calcium tablets may be changed based on these blood test results.

Take atorvastatin calcium tablets each day at any time of day at about the same time each day.

Atorvastatin calcium tablets can be taken with or without food. Don't break atorvastatin calcium

tablets before taking.

Your doctor should start you on a low-fat diet before giving you atorvastatin calcium tablets. Stay

on this low-fat diet when you take atorvastatin calcium tablets.

If you miss a dose of atorvastatin calcium tablets, take it as soon as you remember. Do not take

atorvastatin calcium tablets if it has been more than 12 hours since you missed your last dose. Wait

and take the next dose at your regular time. Do not take 2 doses of atorvastatin calcium tablets at the

same time.

If you take too much atorvastatin calcium tablets or overdose, call your doctor or Poison Control

Center right away. Or go to the nearest emergency room.

What Should I Avoid While Taking Atorvastatin Calcium Tablets?

Talk to your doctor before you start any new medicines. This includes prescription and non-

prescription medicines, vitamins, and herbal supplements. Atorvastatin calcium tablets and certain

other medicines can interact causing serious side effects.

Do not get pregnant. If you get pregnant, stop taking atorvastatin calcium tablets right away and call

your doctor.

What are the Possible Side Effects of Atorvastatin Calcium Tablets?

Atorvastatin calcium tablets can cause serious side effects. These side effects have happened

only to a small number of people. Your doctor can monitor you for them. These side effects

usually go away if your dose is lowered or atorvastatin calcium tablets are stopped. These

serious side effects include:

Muscle problems. Atorvastatin calcium tablets can cause serious muscle problems that can lead to

kidney problems, including kidney failure. You have a higher chance for muscle problems if you are

taking certain other medicines with atorvastatin calcium tablets.

Liver problems. Your doctor should do blood tests to check your liver before you start taking

atorvastatin calcium tablets and if you have symptoms of liver problems while you take atorvastatin

calcium tablets. Call your doctor right away if you have the following symptoms of liver problems:

feel tired or weak

loss of appetite

upper belly pain

dark amber colored urine

yellowing of your skin or the whites of your eyes

Call your doctor right away if you have:

muscle problems like weakness, tenderness, or pain that happen without a good reason, especially if

you also have a fever or feel more tired than usual. This may be an early sign of a rare muscle

problem.

muscle problems that do not go away even after your doctor has advised you to stop taking

atorvastatin calcium tablets. Your doctor may do further tests to diagnose the cause of your muscle

problems.

allergic reactions including swelling of the face, lips, tongue, and/or throat that may cause difficulty

in breathing or swallowing which may require treatment right away.

nausea and vomiting.

passing brown or dark-colored urine.

you feel more tired than usual

your skin and whites of your eyes get yellow.

stomach pain.

allergic skin reactions.

In clinical studies, patients reported the following common side effects while taking atorvastatin

calcium tablets: diarrhea, upset stomach, muscle and joint pain, and alterations in some laboratory blood

tests.

The following additional side effects have been reported with atorvastatin calcium tablets: tiredness,

tendon problems, memory loss, and confusion.

Talk to your doctor or pharmacist if you have side effects that bother you or that will not go away.

These are not all the side effects of atorvastatin calcium tablets. Ask your doctor or pharmacist for a

complete list.

How do I store Atorvastatin Calcium Tablets

Store atorvastatin calcium tablets at room temperature, 68°F to 77°F (20°C to 25°C).

Do not keep medicine that is out of date or that you no longer need.

Keep atorvastatin calcium tablets and all medicines out of the reach of children. Be sure that if

you throw medicine away, it is out of the reach of children.

General Information About Atorvastatin Calcium Tablets

Medicines are sometimes prescribed for conditions that are not mentioned in patient information leaflets.

Do not use atorvastatin calcium tablets for a condition for which it was not prescribed. Do not give

atorvastatin calcium tablets to other people, even if they have the same problem you have. It may harm

them.

This leaflet summarizes the most important information about atorvastatin calcium tablets. If you would

like more information, talk with your doctor. You can ask your doctor or pharmacist for information

about atorvastatin calcium tablets that is written for health professionals. Or for more information

contact Apotex Corp., Drug Safety at 1-800-706-5575.

What are the Ingredients In Atorvastatin Calcium Tablets?

Active Ingredient: atorvastatin calcium

Inactive Ingredients: calcium acetate, colloidal silicon dioxide, croscarmellose sodium,

hydroxypropyl cellulose, hypromellose, magnesium stearate (vegetable source), microcrystalline

cellulose, polyethylene glycol, sodium carbonate, and titanium dioxide.

APOTEX INC.

ATORVASTATIN CALCIUM TABLETS, USP

10 mg, 20 mg, 40 mg, and 80 mg

Manufactured By

Manufactured For

Apotex Inc.

Apotex Corp.

Toronto, Ontario

Weston, Florida

Toronto, Ontario

Weston, Florida

Canada, M9L 1T9

33326

Revised: May 2019

Rev. 16

Atorvastatin Calcium 10mg Tablet

ATORVASTATIN CALCIUM 20MG TABLET

ATORVASTATIN CALCIUM

atorvastatin calcium tablet, film coated

Product Information

Product T ype

HUMAN PRESCRIPTION

DRUG

Ite m Code

(S ource )

NDC:6 36 29 -479 6 (NDC:6 0 50 5-

2578 )

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of

Stre ng th

Stre ng th

ATO RVASTATIN CALCIUM TRIHYDRATE (UNII: 48 A5M73Z4Q) (ATORVASTATIN -

UNII:A0 JWA8 5V8 F)

ATORVASTATIN

10 mg

Inactive Ingredients

Ingredient Name

Stre ng th

CALCIUM ACETATE (UNII: Y8 8 2YXF34X)

CRO SCARMELLO SE SO DIUM (UNII: M28 OL1HH48 )

SO DIUM CARBO NATE (UNII: 45P326 1C7T)

MICRO CRYSTALLINE CELLULO SE (UNII: OP1R32D6 1U)

MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 )

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4)

HYPRO MELLO SE, UNSPECIFIED (UNII: 3NXW29 V3WO)

HYDRO XYPRO PYL CELLULO SE ( 16 0 0 0 0 0 WAMW) (UNII: RFW2ET6 71P)

PO LYETHYLENE GLYCO L 8 0 0 0 (UNII: Q6 6 2QK8 M3B)

TITANIUM DIO XIDE (UNII: 15FIX9 V2JP)

Product Characteristics

Color

WHITE

S core

no sco re

S hap e

OVAL

S iz e

9 mm

Flavor

Imprint Code

APO;A10

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 36 29 -479 6 -1

30 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 12

0 9 /30 /20 17

2

NDC:6 36 29 -479 6 -2

9 0 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 12

0 9 /30 /20 17

3

NDC:6 36 29 -479 6 -3

6 0 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 12

0 9 /30 /20 17

4

NDC:6 36 29 -479 6 -4

120 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 12

0 9 /30 /20 17

5

NDC:6 36 29 -479 6 -5

10 0 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 12

0 9 /30 /20 17

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

ANDA

ANDA0 9 0 548

0 5/29 /20 12

0 9 /30 /20 17

ATORVASTATIN CALCIUM

atorvastatin calcium tablet, film coated

Product Information

Product T ype

HUMAN PRESCRIPTION

DRUG

Ite m Code

(S ource )

NDC:6 36 29 -8 0 32(NDC:6 0 50 5-

2579 )

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of

Stre ng th

Stre ng th

ATO RVASTATIN CALCIUM TRIHYDRATE (UNII: 48 A5M73Z4Q) (ATORVASTATIN -

UNII:A0 JWA8 5V8 F)

ATORVASTATIN

20 mg

Inactive Ingredients

Ingredient Name

Stre ng th

CALCIUM ACETATE (UNII: Y8 8 2YXF34X)

CRO SCARMELLO SE SO DIUM (UNII: M28 OL1HH48 )

SO DIUM CARBO NATE (UNII: 45P326 1C7T)

MICRO CRYSTALLINE CELLULO SE (UNII: OP1R32D6 1U)

MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 )

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4)

HYPRO MELLO SE, UNSPECIFIED (UNII: 3NXW29 V3WO)

HYDRO XYPRO PYL CELLULO SE ( 16 0 0 0 0 0 WAMW) (UNII: RFW2ET6 71P)

PO LYETHYLENE GLYCO L 8 0 0 0 (UNII: Q6 6 2QK8 M3B)

TITANIUM DIO XIDE (UNII: 15FIX9 V2JP)

Product Characteristics

Color

WHITE

S core

no sco re

S hap e

OVAL

S iz e

11mm

Flavor

Imprint Code

APO;ATV20

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 36 29 -8 0 32-1

30 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

0 7/25/20 19

2

NDC:6 36 29 -8 0 32-2

9 0 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

0 7/25/20 19

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

ANDA

ANDA0 9 0 548

0 5/29 /20 12

Labeler -

Bryant Ranch Prepack (171714327)

Establishment

Bryant Ranch Prepack

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Bryant Ranch Prepack

171714327

REPACK(6 36 29 -8 0 32, 6 36 29 -479 6 ) , RELABEL(6 36 29 -479 6 , 6 36 29 -8 0 32)

Revised: 8/2019

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