| NDC Code | 43063-522-24 |
|---|
| Package Description | 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-522-24) |
|---|
| Product NDC | 43063-522 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Atovaquone And Proguanil Hcl |
|---|
| Non-Proprietary Name | Atovaquone And Proguanil Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120727 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA021078 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | ATOVAQUONE; PROGUANIL HYDROCHLORIDE |
|---|
| Strength | 250; 100 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Antimalarial [EPC], Antimalarial [EPC], Antiprotozoal [EPC], Dihydrofolate Reductase Inhibitors [MoA] |
|---|