| NDC Code | 52959-969-03 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-969-03) |
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| Product NDC | 52959-969 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Truvada |
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| Non-Proprietary Name | Emtricitabine And Tenofovir Disoproxil Fumarate |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20040802 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021752 |
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| Manufacturer | H.J. Harkins Company, Inc. |
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| Substance Name | EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE |
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| Strength | 200; 300 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC] |
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