| NDC Code | 60687-366-25 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-366-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-366-95) |
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| Product NDC | 60687-366 |
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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 | 20180501 |
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| End Marketing Date | 20200331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090647 |
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| Manufacturer | American Health Packaging |
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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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