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Bisoprolol Fumarate - 59762-1261-2 - (Bisoprolol Fumarate)

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Drug Information of Bisoprolol Fumarate

Product NDC: 59762-1261
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: 59762-1261
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077910
Marketing Category: ANDA
Start Marketing Date: 20061227

Package Information of Bisoprolol Fumarate

Package NDC: 59762-1261-2
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (59762-1261-2)

NDC Information of Bisoprolol Fumarate

NDC Code 59762-1261-2
Proprietary Name Bisoprolol Fumarate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (59762-1261-2)
Product NDC 59762-1261
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bisoprolol Fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061227
Marketing Category Name ANDA
Labeler Name Greenstone LLC
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


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