TRIAMTERENE AND HYDROCHLOROTHIAZIDE tablet

Država: Združene države Amerike

Jezik: angleščina

Source: NLM (National Library of Medicine)

Aktivna sestavina:

TRIAMTERENE (UNII: WS821Z52LQ) (TRIAMTERENE - UNII:WS821Z52LQ), HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (HYDROCHLOROTHIAZIDE - UNII:0J48LPH2TH)

Dostopno od:

Bryant Ranch Prepack

INN (mednarodno ime):

TRIAMTERENE

Sestava:

TRIAMTERENE 37.5 mg

Pot uporabe:

ORAL

Tip zastaranja:

PRESCRIPTION DRUG

Terapevtske indikacije:

This fixed combination drug is not indicated for the initial therapy of edema or hypertension except in individuals in whom the development of hypokalemia cannot be risked. Triamterene and hydrochlorothiazide tablets, USP may be used alone or in combination with other antihypertensive drugs, such as beta-blockers. Since triamterene and hydrochlorothiazide tablets may enhance the actions of these drugs, dosage adjustments may be necessary. The routine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unnecessary hazard. Diuretics do not prevent development of toxemia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of developed toxemia. Edema during pregnancy may arise from pathological causes or from the physiologic and mechanical consequences of pregnancy. Thiazides are indicated in pregnancy when edema is due to pathologic causes, just as they are in the absence of pregnancy. Dependent edema in pregnancy, resulting from r

Povzetek izdelek:

Product: 63629-6404 NDC: 63629-6404-1 30 TABLET in a BOTTLE Product: 63629-6712 NDC: 63629-6712-1 30 TABLET in a BOTTLE

Status dovoljenje:

New Drug Application

Lastnosti izdelka

TRIAMTERENE AND HYDROCHLOROTHIAZIDE- TRIAMTERENE AND
HYDROCHLOROTHIAZIDE TABLET
BRYANT RANCH PREPACK
----------
DESCRIPTION
Triamterene and hydrochlorothiazide combines triamterene, a
potassium-conserving
diuretic, with the natriuretic agent, hydrochlorothiazide.
Each Triamterene and Hydrochlorothiazide Tablet, USP 37.5 mg/25 mg
contains:
Triamterene, USP . . . . . . . . 37.5 mg
Hydrochlorothiazide, USP . . . 25 mg
Each Triamterene and Hydrochlorothiazide Tablet, USP 75 mg/50 mg
contains:
Triamterene, USP . . . . . . . . . . 75 mg
Hydrochlorothiazide, USP . . . . 50 mg
Triamterene and hydrochlorothiazide tablets for oral administration
contain the following
inactive ingredients: colloidal silicon dioxide, croscarmellose
sodium, D&C Yellow No. 10
Aluminum Lake, magnesium stearate, microcrystalline cellulose,
powdered cellulose and
sodium lauryl sulfate. Additionally, the 37.5 mg/25 mg product
contains FD&C Blue No. 1
Aluminum Lake.
Triamterene is 2,4,7-triamino-6-phenylpteridine. Triamterene is
practically insoluble in
water, benzene, chloroform, ether and dilute alkali hydroxides. It is
soluble in formic acid
and sparingly soluble in methoxyethanol. Triamterene is very slightly
soluble in acetic
acid, alcohol and dilute mineral acids. Its molecular weight is
253.27. Its structural
formula is:
Hydrochlorothiazide is 6-chloro-3,4-dihydro-2_H_-1,2,4,
benzothiadiazine-7-sulfonamide
1,1-dioxide. Hydrochlorothiazide is slightly soluble in water and
freely soluble in sodium
hydroxide solution, n-butylamine and dimethylformamide. It is
sparingly soluble in
methanol and insoluble in ether, chloroform and dilute mineral acids.
Its molecular weight
is 297.73. Its structural formula is:
CLINICAL PHARMACOLOGY
Triamterene and hydrochlorothiazide is a diuretic, antihypertensive
drug product,
principally due to its hydrochlorothiazide component; the triamterene
component
reduces the excessive potassium loss which may occur with
hydrochlorothiazide use.
HYDROCHLOROTHIAZIDE
Hydrochlorothiazide is a diuretic and antihypertensive ag