| NDC Code | 58118-0404-4 |
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| Package Description | 24 TABLET, FILM COATED in 1 BOTTLE (58118-0404-4) |
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| Product NDC | 58118-0404 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Atovaquone And Proguanil Hydrochloride |
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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 | 20110818 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091211 |
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| Manufacturer | Clinical Solutions Wholesale |
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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],Antiprotozoal [EPC],Antimalarial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
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