Lamivudine and Zidovudine (PD-Rx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Lamivudine and Zidovudine drug offered from PD-Rx Pharmaceuticals, 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: | PD-Rx Pharmaceuticals, 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 PD-Rx Pharmaceuticals, Inc. |
| LABELER NAME: | PD-Rx Pharmaceuticals, 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: | 43063-346_52a4248b-01a1-2938-e054-00144ff88e88 |
| PRODUCT NDC: | 43063-346 |
| APPLICATION NUMBER: | ANDA079081 |
Other LAMIVUDINE; ZIDOVUDINE Pharmaceutical Manufacturers / Labelers:
