| Product NDC: | 63629-1596 |
| Proprietary Name: | PLENDIL |
| Non Proprietary Name: | Felodipine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Felodipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63629-1596 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019834 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19910916 |
| Package NDC: | 63629-1596-2 |
| Package Description: | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1596-2) |
| NDC Code | 63629-1596-2 |
| Proprietary Name | PLENDIL |
| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1596-2) |
| Product NDC | 63629-1596 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Felodipine |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19910916 |
| Marketing Category Name | NDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | FELODIPINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |