NDC Code | 43598-744-30 |
Package Description | 30 TABLET in 1 BOTTLE (43598-744-30) |
Product NDC | 43598-744 |
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 | 20181120 |
Marketing Category Name | ANDA |
Application Number | ANDA200909 |
Manufacturer | Dr.Reddys Laboratories Inc |
Substance Name | EZETIMIBE; SIMVASTATIN |
Strength | 10; 20 |
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] |