IBUDONE - hydrocodone bitartrate and ibuprofen
Navigation: NDC > Supplier starting with: P > POLY PHARMACEUTICALS| Field | Value |
|---|---|
| NDC Code: | 50991-579 |
| Proprietary Name: | IBUDONE |
| Suffix: | |
| Non-Proprietary Name: | hydrocodone bitartrate and ibuprofen |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 06-11-2006 |
| Category Name: | ANDA |
| Application Number: | ANDA077723 |
| Labeler: | POLY PHARMACEUTICALS |
| Substance Name: | HYDROCODONE BITARTRATE; IBUPROFEN |
| Active Numerator Strength: | 10; 200 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule: | CIII |