Oxymorphone hydrochloride (Ranbaxy Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Oxymorphone hydrochloride drug offered from Ranbaxy Pharmaceuticals Inc.. 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: | Ranbaxy Pharmaceuticals Inc. |
| 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, FILM COATED, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-04-13 |
| END MARKETING DATE: | 0000-00-00 |
Oxymorphone hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Oxymorphone hydrochloride from Ranbaxy Pharmaceuticals Inc. |
| LABELER NAME: | Ranbaxy Pharmaceuticals Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 5(mg/1) |
| START MARKETING DATE: | 2015-04-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63304-218_b6f91a0b-ca7e-4af1-8ea6-741af2050314 |
| PRODUCT NDC: | 63304-218 |
| APPLICATION NUMBER: | ANDA203506 |
Other OXYMORPHONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
