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Bisoprolol Fumarate - 21695-670-90 - (Bisoprolol fumarate)

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Drug Information of Bisoprolol Fumarate

Product NDC: 21695-670
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
Coding System: National Drug Codes(NDC)

Labeler Information of Bisoprolol Fumarate

Product NDC: 21695-670
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078635
Marketing Category: ANDA
Start Marketing Date: 20090921

Package Information of Bisoprolol Fumarate

Package NDC: 21695-670-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (21695-670-90)

NDC Information of Bisoprolol Fumarate

NDC Code 21695-670-90
Proprietary Name Bisoprolol Fumarate
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (21695-670-90)
Product NDC 21695-670
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bisoprolol fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090921
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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