| NDC Code | 43598-585-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (43598-585-05) |
|---|
| Product NDC | 43598-585 |
|---|
| 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 | 20170426 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200909 |
|---|
| Manufacturer | Dr.Reddys Laboratories Inc |
|---|
| 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] |
|---|