| Product NDC: | 55154-5979 |
| Proprietary Name: | nifedipine |
| Non Proprietary Name: | nifedipine |
| Active Ingredient(s): | 10 mg/1 & nbsp; nifedipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-5979 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072579 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19910108 |
| Package NDC: | 55154-5979-0 |
| Package Description: | 10 POUCH in 1 BAG (55154-5979-0) > 1 CAPSULE, LIQUID FILLED in 1 POUCH |
| NDC Code | 55154-5979-0 |
| Proprietary Name | nifedipine |
| Package Description | 10 POUCH in 1 BAG (55154-5979-0) > 1 CAPSULE, LIQUID FILLED in 1 POUCH |
| Product NDC | 55154-5979 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nifedipine |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 19910108 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | NIFEDIPINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |