| NDC Code | 0093-5173-01 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5173-01) |
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| Product NDC | 0093-5173 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nifedipine |
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| Non-Proprietary Name | Nifedipine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20001211 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075289 |
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| Manufacturer | Teva Pharmaceuticals USA Inc |
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| Substance Name | NIFEDIPINE |
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| Strength | 60 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS] |
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