| NDC Code | 70807-503-12 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-12) |
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| Product NDC | 70807-503 |
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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 | 20211015 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212016 |
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| Manufacturer | Elite Pharmaceutical Solution, Inc. |
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| Substance Name | NIFEDIPINE |
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| Strength | 90 |
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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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