| NDC Code | 47335-410-22 |
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| Package Description | 9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22) |
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| Product NDC | 47335-410 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sumatriptan And Naproxen Sodium |
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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 | 20180720 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202803 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE |
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| Strength | 500; 85 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
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