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Bisoprolol Fumarate - 65862-087-30 - (Bisoprolol Fumarate)

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Drug Information of Bisoprolol Fumarate

Product NDC: 65862-087
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: 65862-087
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077910
Marketing Category: ANDA
Start Marketing Date: 20061227

Package Information of Bisoprolol Fumarate

Package NDC: 65862-087-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (65862-087-30)

NDC Information of Bisoprolol Fumarate

NDC Code 65862-087-30
Proprietary Name Bisoprolol Fumarate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (65862-087-30)
Product NDC 65862-087
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 Aurobindo Pharma Limited
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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