| NDC Code | 68071-3910-3 |
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| Package Description | 3 TABLET, FILM COATED in 1 BOTTLE (68071-3910-3) |
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| Product NDC | 68071-3910 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Darunavir |
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| Non-Proprietary Name | Darunavir |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20231128 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210677 |
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| Manufacturer | NuCare Pharmaceuticals, Inc. |
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| Substance Name | DARUNAVIR PROPYLENE GLYCOLATE |
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| Strength | 800 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], HIV Protease Inhibitors [MoA], Protease Inhibitor [EPC] |
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