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bisoprolol fumarate - 0185-0774-30 - (bisoprolol fumarate)

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Drug Information of bisoprolol fumarate

Product NDC: 0185-0774
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of bisoprolol fumarate

Product NDC: 0185-0774
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075643
Marketing Category: ANDA
Start Marketing Date: 20001116

Package Information of bisoprolol fumarate

Package NDC: 0185-0774-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (0185-0774-30)

NDC Information of bisoprolol fumarate

NDC Code 0185-0774-30
Proprietary Name bisoprolol fumarate
Package Description 30 TABLET, COATED in 1 BOTTLE (0185-0774-30)
Product NDC 0185-0774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bisoprolol fumarate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20001116
Marketing Category Name ANDA
Labeler Name Eon Labs, 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


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