| NDC Code | 66582-321-27 |
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| Package Description | 4 POUCH in 1 CARTON (66582-321-27) > 1 BLISTER PACK in 1 POUCH (66582-321-11) > 7 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 66582-321 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Liptruzet |
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| Non-Proprietary Name | Ezetimibe And Atorvastatin |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20130503 |
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| Marketing Category Name | NDA |
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| Application Number | NDA200153 |
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| Manufacturer | Merck Sharp & Dohme Corp. |
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| Substance Name | EZETIMIBE; ATORVASTATIN CALCIUM |
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| Strength | 10; 20 |
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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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