| NDC Code | 0093-9175-01 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-9175-01) |
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| Product NDC | 0093-9175 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Quinidine Sulfate |
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| Non-Proprietary Name | Quinidine Sulfate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 19950101 |
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| End Marketing Date | 20160331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040045 |
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| Manufacturer | Teva Pharmaceuticals USA Inc |
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| Substance Name | QUINIDINE SULFATE |
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| Strength | 300 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antiarrhythmic [EPC],Cytochrome P450 2D6 Inhibitor [EPC],Cytochrome P450 2D6 Inhibitors [MoA] |
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