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Bisoprolol Fumarate and Hydrochlorothiazide - 63629-1674-1 - (Bisoprolol Fumarate and Hydrochlorothiazide)

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Drug Information of Bisoprolol Fumarate and Hydrochlorothiazide

Product NDC: 63629-1674
Proprietary Name: Bisoprolol Fumarate and Hydrochlorothiazide
Non Proprietary Name: Bisoprolol Fumarate and Hydrochlorothiazide
Active Ingredient(s): 2.5; 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: 63629-1674
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075579
Marketing Category: ANDA
Start Marketing Date: 20000925

Package Information of Bisoprolol Fumarate and Hydrochlorothiazide

Package NDC: 63629-1674-1
Package Description: 100 TABLET, COATED in 1 BOTTLE (63629-1674-1)

NDC Information of Bisoprolol Fumarate and Hydrochlorothiazide

NDC Code 63629-1674-1
Proprietary Name Bisoprolol Fumarate and Hydrochlorothiazide
Package Description 100 TABLET, COATED in 1 BOTTLE (63629-1674-1)
Product NDC 63629-1674
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bisoprolol Fumarate and Hydrochlorothiazide
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20000925
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Strength Number 2.5; 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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