| NDC Code | 43063-522-20 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-522-20) |
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| Product NDC | 43063-522 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Atovaquone And Proguanil Hcl |
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| Non-Proprietary Name | Atovaquone And Proguanil Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20120727 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021078 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | ATOVAQUONE; PROGUANIL HYDROCHLORIDE |
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| Strength | 250; 100 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Antimalarial [EPC], Antimalarial [EPC], Antiprotozoal [EPC], Dihydrofolate Reductase Inhibitors [MoA] |
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