| NDC Code | 58118-0404-1 |
|---|
| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (58118-0404-1) |
|---|
| Product NDC | 58118-0404 |
|---|
| 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 | Clinical Solutions Wholesale |
|---|
| 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] |
|---|