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Zebeta
Zebeta - 51285-061-01 - (Bisoprolol Fumarate)
Drug Information of Zebeta
| 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) |
Labeler Information of Zebeta
| 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 Information of Zebeta
| Package NDC: | 51285-061-01 |
| Package Description: | 30 TABLET in 1 BOTTLE (51285-061-01) |
NDC Information of Zebeta
| 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] |
