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METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE - 54868-5524-0 - (metoprolol tartrate and hydrochlorothiazide)

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Drug Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE

Product NDC: 54868-5524
Proprietary Name: METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
Non Proprietary Name: metoprolol tartrate and hydrochlorothiazide
Active Ingredient(s): 25; 100    mg/1; mg/1 & nbsp;   metoprolol tartrate and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE

Product NDC: 54868-5524
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076792
Marketing Category: ANDA
Start Marketing Date: 20060207

Package Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE

Package NDC: 54868-5524-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-5524-0)

NDC Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE

NDC Code 54868-5524-0
Proprietary Name METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-5524-0)
Product NDC 54868-5524
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate and hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060207
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE
Strength Number 25; 100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE


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