Lamivudine (Silarx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Lamivudine drug offered from Silarx 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] 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: | Silarx Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Lamivudine |
| SUBSTANCE NAME: | LAMIVUDINE |
| 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] |
| ROUTE: | ORAL |
| DOSAGE FORM: | SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2014-01-30 |
| END MARKETING DATE: | 0000-00-00 |
Lamivudine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Lamivudine from Silarx Pharmaceuticals, Inc. |
| LABELER NAME: | Silarx Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2014-01-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 54838-566_2e32a1ee-930a-48cd-8f71-6926af473558 |
| PRODUCT NDC: | 54838-566 |
| APPLICATION NUMBER: | ANDA203564 |
Other LAMIVUDINE Pharmaceutical Manufacturers / Labelers:
