NDC Code | 60219-1157-9 |
Package Description | 90 TABLET in 1 BOTTLE (60219-1157-9) |
Product NDC | 60219-1157 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ezetimibe And Simvastatin |
Non-Proprietary Name | Ezetimibe And Simvastatin |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20171121 |
Marketing Category Name | ANDA |
Application Number | ANDA208831 |
Manufacturer | Amneal Pharmaceuticals NY LLC |
Substance Name | EZETIMIBE; SIMVASTATIN |
Strength | 10; 40 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |