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Nifedipine
Nifedipine - 63739-805-43 - (Nifedipine)
Drug Information of Nifedipine
| Product NDC: | 63739-805 |
| 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) |
Labeler Information of Nifedipine
| Product NDC: | 63739-805 |
| Labeler Name: | McKesson Packaging Servives a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077899 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110701 |
Package Information of Nifedipine
| Package NDC: | 63739-805-43 |
| Package Description: | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63739-805-43) |
NDC Information of Nifedipine
| NDC Code | 63739-805-43 |
| Proprietary Name | Nifedipine |
| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63739-805-43) |
| Product NDC | 63739-805 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nifedipine |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Servives a business unit of McKesson Corporation |
| Substance Name | NIFEDIPINE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
