| NDC Code | 62559-700-90 |
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| Package Description | 90 TABLET in 1 BOTTLE (62559-700-90) |
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| Product NDC | 62559-700 |
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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 | 20180924 |
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| End Marketing Date | 20230331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208831 |
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| Manufacturer | ANI Pharmaceuticals, Inc. |
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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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