Product NDC: | 51285-061 |
Proprietary Name: | Zebeta |
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) |
Product NDC: | 51285-061 |
Labeler Name: | Duramed Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019982 |
Marketing Category: | NDA |
Start Marketing Date: | 19920731 |
Package NDC: | 51285-061-01 |
Package Description: | 30 TABLET in 1 BOTTLE (51285-061-01) |
NDC Code | 51285-061-01 |
Proprietary Name | Zebeta |
Package Description | 30 TABLET in 1 BOTTLE (51285-061-01) |
Product NDC | 51285-061 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Bisoprolol Fumarate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19920731 |
Marketing Category Name | NDA |
Labeler Name | Duramed Pharmaceuticals, Inc. |
Substance Name | BISOPROLOL FUMARATE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |