| NDC Code | 68682-108-10 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-10) |
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| Product NDC | 68682-108 |
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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 | 20000927 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075289 |
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| Manufacturer | Oceanside Pharmaceuticals |
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| Substance Name | NIFEDIPINE |
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| Strength | 30 |
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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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