Lamivudine and Zidovudine (H.J. Harkins Company, Inc.)
Welcome to the PulseAid listing for the Lamivudine and Zidovudine drug offered from H.J. Harkins Company, Inc.. This 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],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | H.J. Harkins Company, Inc. |
NON-PROPRIETARY NAME: | Lamivudine and Zidovudine |
SUBSTANCE NAME: | LAMIVUDINE; ZIDOVUDINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | 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],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2011-12-27 |
END MARKETING DATE: | 0000-00-00 |
Lamivudine and Zidovudine HUMAN PRESCRIPTION DRUG Details:
Item Description | Lamivudine and Zidovudine from H.J. Harkins Company, Inc. |
LABELER NAME: | H.J. Harkins Company, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 150; 300(mg/1; mg/1) |
START MARKETING DATE: | 2011-12-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 76519-1005_dae1ab04-6614-4083-b7b6-2612c4be0fe2 |
PRODUCT NDC: | 76519-1005 |
APPLICATION NUMBER: | ANDA079081 |
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