NDC Code | 68462-233-11 |
Package Description | 10 BLISTER PACK in 1 CARTON (68462-233-11) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 68462-233 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Felodipine |
Non-Proprietary Name | Felodipine |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20101220 |
Marketing Category Name | ANDA |
Application Number | ANDA090365 |
Manufacturer | Glenmark Pharmaceuticals Inc., USA |
Substance Name | FELODIPINE |
Strength | 2.5 |
Strength Unit | mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |