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Bisoprolol Fumarate and Hydrochlorothiazide - 54868-4576-0 - (Bisoprolol Fumarate and Hydrochlorothiazide)

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Drug Information of Bisoprolol Fumarate and Hydrochlorothiazide

Product NDC: 54868-4576
Proprietary Name: Bisoprolol Fumarate and Hydrochlorothiazide
Non Proprietary Name: Bisoprolol Fumarate and Hydrochlorothiazide
Active Ingredient(s): 5; 6.25    mg/1; mg/1 & nbsp;   Bisoprolol Fumarate and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Bisoprolol Fumarate and Hydrochlorothiazide

Product NDC: 54868-4576
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075579
Marketing Category: ANDA
Start Marketing Date: 20020115

Package Information of Bisoprolol Fumarate and Hydrochlorothiazide

Package NDC: 54868-4576-0
Package Description: 30 TABLET, COATED in 1 BOTTLE (54868-4576-0)

NDC Information of Bisoprolol Fumarate and Hydrochlorothiazide

NDC Code 54868-4576-0
Proprietary Name Bisoprolol Fumarate and Hydrochlorothiazide
Package Description 30 TABLET, COATED in 1 BOTTLE (54868-4576-0)
Product NDC 54868-4576
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bisoprolol Fumarate and Hydrochlorothiazide
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20020115
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Strength Number 5; 6.25
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 Bisoprolol Fumarate and Hydrochlorothiazide


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