Oxymorphone Hydrochloride (Aurolife Pharma, LLC)
Welcome to the PulseAid listing for the Oxymorphone Hydrochloride drug offered from Aurolife Pharma, 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: | Aurolife Pharma, 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: | 2016-04-26 |
END MARKETING DATE: | 0000-00-00 |
Oxymorphone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxymorphone Hydrochloride from Aurolife Pharma, LLC |
LABELER NAME: | Aurolife Pharma, LLC |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 2016-04-26 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 13107-103_37c90785-5131-4f33-911c-2e5183c4b127 |
PRODUCT NDC: | 13107-103 |
APPLICATION NUMBER: | ANDA204459 |
Other OXYMORPHONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: