| NDC Code | 52959-738-02 |
|---|
| Package Description | 120 TABLET in 1 BOTTLE (52959-738-02) |
|---|
| Product NDC | 52959-738 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydrocodone Bitartrate And Ibuprofen |
|---|
| Non-Proprietary Name | Hydrocodone Bitartrate And Ibuprofen |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100118 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076642 |
|---|
| Manufacturer | H.J. Harkins Company, Inc. |
|---|
| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
|---|
| Strength | 7.5; 200 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|
| DEA Schedule | CIII |
|---|