Oxymorphone hydrochloride (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Oxymorphone hydrochloride drug offered from Actavis Pharma, 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: | Actavis Pharma, 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, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-12-31 |
END MARKETING DATE: | 0000-00-00 |
Oxymorphone hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxymorphone hydrochloride from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 2010-12-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0228-3227_961a3eee-3fac-44c7-aee5-1c49459174b0 |
PRODUCT NDC: | 0228-3227 |
APPLICATION NUMBER: | ANDA079046 |
Other OXYMORPHONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: