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Nifedical
Nifedical - 63629-1559-2 - (nifedipine)
Drug Information of Nifedical
| Product NDC: | 63629-1559 |
| Proprietary Name: | Nifedical |
| Non Proprietary Name: | nifedipine |
| Active Ingredient(s): | 30 mg/1 & nbsp; nifedipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nifedical
| Product NDC: | 63629-1559 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075289 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010209 |
Package Information of Nifedical
| Package NDC: | 63629-1559-2 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-1559-2) |
NDC Information of Nifedical
| NDC Code | 63629-1559-2 |
| Proprietary Name | Nifedical |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-1559-2) |
| Product NDC | 63629-1559 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nifedipine |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20010209 |
| 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] |
