| NDC Code | 63379-039-01 |
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| Package Description | 9 TABLET, FILM COATED in 1 BOTTLE (63379-039-01) |
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| Product NDC | 63379-039 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Treximet |
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| Non-Proprietary Name | Sumatriptan And Naproxen Sodium |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20080425 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA021926 |
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| Manufacturer | Glaxo Operations UK Ltd |
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| Substance Name | SUMATRIPTAN SUCCINATE; NAPROXEN SODIUM |
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| Strength | 85; 500 |
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| Strength Unit | mg/1; mg/1 |
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| 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] |
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