| NDC Code | 68462-321-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE (68462-321-10) |
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| Product NDC | 68462-321 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ezetimibe And Simvastatin |
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| Non-Proprietary Name | Ezetimibe And Simvastatin |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20190627 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208699 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | EZETIMIBE; SIMVASTATIN |
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| Strength | 10; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
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