| NDC Code: |
0555-0778 |
| Proprietary Name: |
Oxycodone Hydrochloride and Ibuprofen |
| Suffix: |
|
| Non-Proprietary Name: |
Oxycodone Hydrochloride and Ibuprofen |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
04-12-2007 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078316 |
| Labeler: |
BARR 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 |
