| NDC Code | 60687-291-32 |
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| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-291-32) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-291-33) |
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| Product NDC | 60687-291 |
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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 | 20170425 |
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| End Marketing Date | 20190131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077899 |
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| Manufacturer | American Health Packaging |
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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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