HYDROCODONE BITARTRATE AND IBUPROFEN - HYDROCODONE BITARTRATE AND IBUPROFEN
Navigation: NDC > Supplier starting with: P > PD RX PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 43063-349 |
| Proprietary Name: | HYDROCODONE BITARTRATE AND IBUPROFEN |
| Suffix: | |
| Non-Proprietary Name: | HYDROCODONE BITARTRATE AND IBUPROFEN |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 01-04-2004 |
| Category Name: | ANDA |
| Application Number: | ANDA076604 |
| Labeler: | PD RX PHARMACEUTICALS, INC. |
| Substance Name: | HYDROCODONE BITARTRATE; IBUPROFEN |
| Active Numerator Strength: | 7.5; 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 |