NALTREXONE HYDROCHLORIDE (Sun Pharma Global FZE)
Welcome to the PulseAid listing for the NALTREXONE HYDROCHLORIDE drug offered from Sun Pharma Global FZE. This Opioid Antagonist [EPC],Opioid Antagonists [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: | Sun Pharma Global FZE |
| NON-PROPRIETARY NAME: | NALTREXONE HYDROCHLORIDE |
| SUBSTANCE NAME: | NALTREXONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2012-02-29 |
| END MARKETING DATE: | 0000-00-00 |
NALTREXONE HYDROCHLORIDE HUMAN PRESCRIPTION DRUG Details:
| Item Description | NALTREXONE HYDROCHLORIDE from Sun Pharma Global FZE |
| LABELER NAME: | Sun Pharma Global FZE |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/1) |
| START MARKETING DATE: | 2012-02-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 47335-326_64cc17e8-ff8f-463e-aca3-5e85f3f4ec0a |
| PRODUCT NDC: | 47335-326 |
| APPLICATION NUMBER: | ANDA090356 |
Other NALTREXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
