Naloxone Hydrochloride (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the Naloxone Hydrochloride drug offered from REMEDYREPACK INC.. 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: | REMEDYREPACK INC. |
| NON-PROPRIETARY NAME: | Naloxone Hydrochloride |
| SUBSTANCE NAME: | NALOXONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| ROUTE: | PARENTERAL |
| DOSAGE FORM: | INJECTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2017-10-18 |
| END MARKETING DATE: | 0000-00-00 |
Naloxone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Naloxone Hydrochloride from REMEDYREPACK INC. |
| LABELER NAME: | REMEDYREPACK INC. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1(mg/mL) |
| START MARKETING DATE: | 2017-10-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70518-0796_5c515c84-cbfa-513e-e053-2991aa0aaaeb |
| PRODUCT NDC: | 70518-0796 |
| APPLICATION NUMBER: | ANDA072076 |
Other NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
