| NDC Code | 84063-001-04 |
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| Package Description | 1 BOTTLE in 1 CARTON (84063-001-04) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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| Product NDC | 84063-001 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nisoldipine |
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| Non-Proprietary Name | Nisoldipine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20240523 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216606 |
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| Manufacturer | Utopic Pharmaceuticals Inc |
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| Substance Name | NISOLDIPINE |
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| Strength | 8.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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