| NDC Code | 0378-2222-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2222-05) |
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| Product NDC | 0378-2222 |
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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 | 20080725 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079051 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | NISOLDIPINE |
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| Strength | 20 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE] |
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