| NDC Code | 71921-105-33 |
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| Package Description | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (71921-105-33) |
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| Product NDC | 71921-105 |
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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, COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20251126 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209498 |
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| Manufacturer | Florida Pharmaceutical Products, LLC. |
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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 | Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleosides [CS] |
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