Oxymorphone Hydrochloride (CorePharma, LLC)
Welcome to the PulseAid listing for the Oxymorphone Hydrochloride drug offered from CorePharma, LLC. This Full Opioid Agonists [MoA],Opioid Agonist [EPC] 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: | CorePharma, LLC |
| NON-PROPRIETARY NAME: | Oxymorphone Hydrochloride |
| SUBSTANCE NAME: | OXYMORPHONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-01-17 |
| END MARKETING DATE: | 2017-12-31 |
Oxymorphone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Oxymorphone Hydrochloride from CorePharma, LLC |
| LABELER NAME: | CorePharma, LLC |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2015-01-17 |
| END MARKETING DATE: | 2017-12-31 |
| PRODUCT ID: | 64720-259_02ce8356-dee5-4a7d-8d53-60343870697f |
| PRODUCT NDC: | 64720-259 |
| APPLICATION NUMBER: | ANDA201187 |
Other OXYMORPHONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
