Product NDC: | 63629-4089 |
Proprietary Name: | nifedipine |
Non Proprietary Name: | nifedipine |
Active Ingredient(s): | 30 mg/1 & nbsp; nifedipine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-4089 |
Labeler Name: | bryant ranch prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075128 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091005 |
Package NDC: | 63629-4089-1 |
Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4089-1) |
NDC Code | 63629-4089-1 |
Proprietary Name | nifedipine |
Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4089-1) |
Product NDC | 63629-4089 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nifedipine |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20091005 |
Marketing Category Name | ANDA |
Labeler Name | bryant ranch prepack |
Substance Name | NIFEDIPINE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |