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bisoprolol fumarate
bisoprolol fumarate - 68084-487-21 - (bisoprolol fumarate)
Drug Information of bisoprolol fumarate
| Product NDC: | 68084-487 |
| Proprietary Name: | bisoprolol fumarate |
| Non Proprietary Name: | bisoprolol fumarate |
| Active Ingredient(s): | 5 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: | 68084-487 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075643 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110801 |
Package Information of bisoprolol fumarate
| Package NDC: | 68084-487-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-487-21) > 10 TABLET, COATED in 1 BLISTER PACK (68084-487-11) |
NDC Information of bisoprolol fumarate
| NDC Code | 68084-487-21 |
| Proprietary Name | bisoprolol fumarate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-487-21) > 10 TABLET, COATED in 1 BLISTER PACK (68084-487-11) |
| Product NDC | 68084-487 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bisoprolol fumarate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | BISOPROLOL FUMARATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
