Oxymorphone Hydrochloride (Par Pharmaceutical)
Welcome to the PulseAid listing for the Oxymorphone Hydrochloride drug offered from Par Pharmaceutical. 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: | Par Pharmaceutical |
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: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2010-09-29 |
END MARKETING DATE: | 0000-00-00 |
Oxymorphone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxymorphone Hydrochloride from Par Pharmaceutical |
LABELER NAME: | Par Pharmaceutical |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 2010-09-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 60951-794_59aa8319-de00-4282-98ff-98c41ee36748 |
PRODUCT NDC: | 60951-794 |
APPLICATION NUMBER: | NDA021611 |
Other OXYMORPHONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: