| NDC Code | 63379-039-00 |
|---|
| Package Description | 1 TABLET, FILM COATED in 1 BOTTLE (63379-039-00) |
|---|
| Product NDC | 63379-039 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Treximet |
|---|
| Non-Proprietary Name | Sumatriptan And Naproxen Sodium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20080425 |
|---|
| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
|---|
| Application Number | NDA021926 |
|---|
| Manufacturer | Glaxo Operations UK Ltd |
|---|
| Substance Name | SUMATRIPTAN SUCCINATE; NAPROXEN SODIUM |
|---|
| Strength | 85; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|