Zebeta - 51285-061-01 - (Bisoprolol Fumarate)

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Drug Information of Zebeta

Product NDC: 51285-061
Proprietary Name: Zebeta
Non Proprietary Name: Bisoprolol Fumarate
Active Ingredient(s): 10    mg/1 & nbsp;   Bisoprolol Fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zebeta

Product NDC: 51285-061
Labeler Name: Duramed Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019982
Marketing Category: NDA
Start Marketing Date: 19920731

Package Information of Zebeta

Package NDC: 51285-061-01
Package Description: 30 TABLET in 1 BOTTLE (51285-061-01)

NDC Information of Zebeta

NDC Code 51285-061-01
Proprietary Name Zebeta
Package Description 30 TABLET in 1 BOTTLE (51285-061-01)
Product NDC 51285-061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bisoprolol Fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920731
Marketing Category Name NDA
Labeler Name Duramed Pharmaceuticals, Inc.
Substance Name BISOPROLOL FUMARATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Zebeta


General Information