| NDC Code | 76519-1005-6 |
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| Package Description | 6 TABLET, FILM COATED in 1 BOTTLE (76519-1005-6) |
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| Product NDC | 76519-1005 |
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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 | 20111227 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079081 |
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| Manufacturer | H.J. Harkins Company, Inc. |
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| Substance Name | LAMIVUDINE; ZIDOVUDINE |
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| Strength | 150; 300 |
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| Strength Unit | mg/1; 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 [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
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