| NDC Code | 49349-896-12 |
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| Package Description | 8 TABLET, FILM COATED in 1 BLISTER PACK (49349-896-12) |
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| Product NDC | 49349-896 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lamivudine And Zidovudine |
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| Non-Proprietary Name | Lamivudine And Zidovudine |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20130411 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079081 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | LAMIVUDINE |
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| Strength | 150 |
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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 Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
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