Naltrexone Hydrochloride (Aidarex Pharmaceuticals LLC)
Welcome to the PulseAid listing for the Naltrexone Hydrochloride drug offered from Aidarex Pharmaceuticals LLC. 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: | Aidarex Pharmaceuticals LLC |
| 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: | 2013-09-23 |
| END MARKETING DATE: | 0000-00-00 |
Naltrexone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Naltrexone Hydrochloride from Aidarex Pharmaceuticals LLC |
| LABELER NAME: | Aidarex Pharmaceuticals LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/1) |
| START MARKETING DATE: | 2013-09-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 53217-261_9f0d222c-f87f-486b-b186-b09b1173fc9b |
| PRODUCT NDC: | 53217-261 |
| APPLICATION NUMBER: | ANDA075274 |
Other NALTREXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
