Oxycodone hydrochloride and Ibuprofen (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Oxycodone hydrochloride and Ibuprofen drug offered from Actavis Pharma, Inc.. This Full Opioid Agonists [MoA],Opioid Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [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: | Oxycodone hydrochloride and Ibuprofen |
| SUBSTANCE NAME: | OXYCODONE HYDROCHLORIDE; IBUPROFEN |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2008-11-04 |
| END MARKETING DATE: | 0000-00-00 |
Oxycodone hydrochloride and Ibuprofen HUMAN PRESCRIPTION DRUG Details:
| Item Description | Oxycodone hydrochloride and Ibuprofen from Actavis Pharma, Inc. |
| LABELER NAME: | Actavis Pharma, Inc. |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 5; 400(mg/1; mg/1) |
| START MARKETING DATE: | 2008-11-04 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0228-4029_37777ba2-951e-435f-95d6-67c2fe3185dd |
| PRODUCT NDC: | 0228-4029 |
| APPLICATION NUMBER: | ANDA078769 |
Other OXYCODONE HYDROCHLORIDE; IBUPROFEN Pharmaceutical Manufacturers / Labelers:
