| NDC Code | 70518-0918-0 |
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| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0918-0) |
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| Product NDC | 70518-0918 |
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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 | 20171212 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091612 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | TENOFOVIR DISOPROXIL FUMARATE |
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| Strength | 300 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleosides [CS],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
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