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] |