oxycodone hydrochloride and ibuprofen - oxycodone hydrochloride and ibuprofen
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-3494 |
| Proprietary Name: | oxycodone hydrochloride and ibuprofen |
| Suffix: | |
| Non-Proprietary Name: | oxycodone hydrochloride and ibuprofen |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-12-2007 |
| Category Name: | ANDA |
| Application Number: | ANDA078394 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | IBUPROFEN; OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: | 400; 5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule: | CII |