药物信息为METOPROLOL TARTRATEandHYDROCHLOROTHIAZIDETABLETS, USP50 mg/25 mg, 100 mg/25 mg and 100 mg/50 mgBeta Blocker/Diuretic Antihypertensive (Mylan Pharmaceuticals Inc.): DESCRIPTION
- DESCRIPTION
- INDICATIONS AND USAGE
- DOSAGE AND ADMINISTRATION
- HOW SUPPLIED
- 外部链接相关的METOPROLOL TARTRATEandHYDROCHLOROTHIAZIDETABLETS, USP50 mg/25 mg, 100 mg/25 mg and 100 mg/50 mgBeta Blocker/Diuretic Antihypertensive (Mylan Pharmaceuticals Inc.)
Metoprolol Tartrate and Hydrochlorothiazide Tablets, USP have the antihypertensive effect of metoprolol tartrate, a selective beta1-adrenoreceptor blocking agent, and the antihypertensive and diuretic actions of hydrochlorothiazide. It is available as tablets for oral administration. The 50 mg/25 mg tablets contain 50 mg of metoprolol tartrate USP and 25 mg of hydrochlorothiazide USP; the 100 mg/25 mg tablets contain 100 mg of metoprolol tartrate USP and 25 mg of hydrochlorothiazide USP; and the 100 mg/50 mg tablets contain 100 mg of metoprolol tartrate USP and 50 mg of hydrochlorothiazide USP.
Metoprolol tartrate USP is (±)- 1-Isopropylamino-3-[p-(2-methoxyethyl) phenoxy]-2-propanol L-(+)-tartrate (2:1) salt, and its structural formula is:

Metoprolol tartrate USP is a white, crystalline powder. It is very soluble in water; freely soluble in methylene chloride, in chloroform, and in alcohol; slightly soluble in acetone; and insoluble in ether. Its molecular weight is 684.82.
Hydrochlorothiazide is 6-chloro-3, 4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide, and its structural formula is:

Hydrochlorothiazide USP is a white, or practically white, practically odorless, crystalline powder. It is freely soluble in sodium hydroxide solution, in n-butylamine, and in dimethylformamide; sparingly soluble in methanol; slightly soluble in water; and insoluble in ether, in chloroform, and in dilute mineral acids. Its molecular weight is 297.73.
Inactive Ingredients: Anhydrous lactose, colloidal silicon dioxide, croscarmellose sodium, FD&C yellow #6 lake, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch and sodium lauryl sulfate.
- Drug Information Provided by National Library of Medicine (NLM).
