| NDC Code | 0378-8755-59 |
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| Package Description | 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-8755-59) |
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| Product NDC | 0378-8755 |
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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 | 20180904 |
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| End Marketing Date | 20211231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090872 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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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 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
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