| NDC Code | 0677-1979-01 |
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| Package Description | 1 BOTTLE in 1 CARTON (0677-1979-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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| Product NDC | 0677-1979 |
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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 | 20090901 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020356 |
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| Manufacturer | United Research Laboratories, Inc. |
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| Substance Name | NISOLDIPINE |
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| Strength | 17 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE] |
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