| NDC Code | 69025-102-01 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (69025-102-01) |
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| Product NDC | 69025-102 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tenofovir Disoproxil Fumarate |
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| Non-Proprietary Name | 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 | 20180126 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | AIZANT DRUG RESEARCH SOLUTIONS PVT LTD |
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| Substance Name | TENOFOVIR DISOPROXIL FUMARATE |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC] |
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