NDC Code | 68788-6856-1 |
Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6856-1) |
Product NDC | 68788-6856 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Nifedipine |
Non-Proprietary Name | Nifedipine |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20161213 |
Marketing Category Name | ANDA |
Application Number | ANDA077410 |
Manufacturer | Preferred Pharmaceuticals Inc. |
Substance Name | NIFEDIPINE |
Strength | 90 |
Strength Unit | mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS] |