| NDC Code | 68462-404-90 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68462-404-90) |
|---|
| Product NDC | 68462-404 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Atovaquone And Proguanil Hydrochloride |
|---|
| Non-Proprietary Name | Atovaquone And Proguanil Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110818 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091211 |
|---|
| Manufacturer | Glenmark Pharmaceuticals Inc.,USA |
|---|
| Substance Name | ATOVAQUONE; PROGUANIL HYDROCHLORIDE |
|---|
| Strength | 250; 100 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Antimalarial [EPC],Antiprotozoal [EPC],Antimalarial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
|---|