Home > National Drug Code (NDC) > Bisoprolol Fumarate

Bisoprolol Fumarate - 0093-5271-56 - (Bisoprolol Fumarate)

Alphabetical Index


Drug Information of Bisoprolol Fumarate

Product NDC: 0093-5271
Proprietary Name: Bisoprolol Fumarate
Non Proprietary Name: Bisoprolol Fumarate
Active Ingredient(s): 10    mg/1 & nbsp;   Bisoprolol Fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Bisoprolol Fumarate

Product NDC: 0093-5271
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075644
Marketing Category: ANDA
Start Marketing Date: 20040601

Package Information of Bisoprolol Fumarate

Package NDC: 0093-5271-56
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-5271-56)

NDC Information of Bisoprolol Fumarate

NDC Code 0093-5271-56
Proprietary Name Bisoprolol Fumarate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0093-5271-56)
Product NDC 0093-5271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bisoprolol Fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040601
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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 Bisoprolol Fumarate


General Information