IRBESARTAN AND HYDROCHLOROTHIAZIDE tablet

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

IRBESARTAN (UNII: J0E2756Z7N) (IRBESARTAN - UNII:J0E2756Z7N), HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (HYDROCHLOROTHIAZIDE - UNII:0J48LPH2TH)

Disponível em:

Alembic Pharmaceuticals Limited

Via de administração:

ORAL

Tipo de prescrição:

PRESCRIPTION DRUG

Indicações terapêuticas:

Irbesartan and Hydrochlorothiazide Tablets are indicated for the treatment of hypertension. Irbesartan and Hydrochlorothiazide Tablets may be used in patients whose blood pressure is not adequately controlled on monotherapy. Irbesartan and Hydrochlorothiazide Tablets may also be used as initial therapy in patients who are likely to need multiple drugs to achieve their blood pressure goals. The choice of Irbesartan and Hydrochlorothiazide Tablets as initial therapy for hypertension should be based on an assessment of potential benefits and risks. Patients with stage 2 (moderate or severe) hypertension are at relatively high risk for cardiovascular events (such as strokes, heart attacks, and heart failure), kidney failure, and vision problems, so prompt treatment is clinically relevant. The decision to use a combination as initial therapy should be individualized and may be shaped by considerations such as the baseline blood pressure, the target goal, and the incremental likelihood of achieving goal w

Resumo do produto:

Irbesartan and Hydrochlorothiazide Tablets USP are supplied as follows: Irbesartan and Hydrochlorothiazide Tablets USP 150 mg/12.5 mg: Peach coloured mottled, oval shaped, biconvex, uncoated tablets debossed with “L180” on one side and plain on other side. NDC 46708-442-30   bottle of 30 tablets. NDC 46708-442-90   bottle of 90 tablets. NDC 46708-442-91   bottle of 1000 tablets. NDC 46708-442-10    carton of 10 blisters of 10 tablets. Irbesartan and Hydrochlorothiazide Tablets USP 300 mg/12.5 mg: Peach coloured mottled, oval shaped, biconvex, uncoated tablets debossed with “L181” on one side and plain on other side. NDC 46708-443-30   bottle of 30 tablets. NDC 46708-443-90   bottle of 90 tablets. NDC 46708-443-91   bottle of 1000 tablets. NDC 46708-443-10   carton of 10 blisters of 10 tablets. Irbesartan and Hydrochlorothiazide Tablets USP 300 mg/25 mg: Pinkish brown, oval shaped, biconvex, film coated tablets, debossed with “L182” on one side and plain on other side. NDC 46708-444-30   bottle of 30 tablets. NDC 46708-444-90   bottle of 90 tablets. NDC 46708-444-91   bottle of 1000 tablets. NDC 46708-444-10   carton of 10 blisters of 10 tablets. Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature].

Status de autorização:

Abbreviated New Drug Application

Características técnicas

IRBESARTAN AND HYDROCHLOROTHIAZIDE - IRBESARTAN AND
HYDROCHLOROTHIAZIDE TABLET
ALEMBIC PHARMACEUTICALS LIMITED
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REFERENCE LABEL SET ID: 3B7FD8D4-7C8F-4846-AEF7-ED0D320DC229
REFERENCE LABEL SET ID: 1857965B-88C4-4585-8A2A-65F046AB9A4F
REFERENCE LABEL SET ID: CCB34349-D4C5-4DEE-9513-2CF6E11A9793
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HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
IRBESARTAN AND
HYDROCHLOROTHIAZIDE TABLETS SAFELY AND EFFECTIVELY. SEE FULL
PRESCRIBING INFORMATION
FOR IRBESARTAN AND HYDROCHLOROTHIAZIDE TABLETS.
IRBESARTAN AND HYDROCHLOROTHIAZIDE TABLETS, FOR ORAL USE
INITIAL U.S. APPROVAL: 1997
WARNING: FETAL TOXICITY
_SEE FULL PRESCRIBING INFORMATION FOR COMPLETE BOXED WARNING._
WHEN PREGNANCY IS DETECTED, DISCONTINUE IRBESARTAN AND
HYDROCHLOROTHIAZIDE
TABLETS AS SOON AS POSSIBLE. (5.1) DRUGS THAT ACT DIRECTLY ON THE RENIN-ANGIOTENSIN SYSTEM CAN CAUSE
INJURY AND DEATH
TO THE DEVELOPING FETUS. (5.1)
INDICATIONS AND USAGE
Irbesartan and Hydrochlorothiazide Tablets USP is a combination of
irbesartan, an angiotensin II receptor
antagonist, and hydrochlorothiazide, a thiazide diuretic, indicated
for hypertension: (1)
In patients not adequately controlled with monotherapy. (1)
As initial therapy in patients likely to need multiple drugs to
achieve their blood pressure goals. (1)
DOSAGE AND ADMINISTRATION
GENERAL CONSIDERATIONS (2)
Maximum effects within 2 to 4 weeks after dose change. (2.1)
Renal impairment: Not recommended for patients wit