| NDC Code | 70748-215-07 |
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| Package Description | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (70748-215-07) |
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| Product NDC | 70748-215 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Naproxen And Esomeprazole Magnesium |
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| Non-Proprietary Name | Naproxen And Esomeprazole Magnesium |
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| Dosage Form | TABLET, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20200304 |
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| End Marketing Date | 20240930 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA022511 |
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| Manufacturer | Lupin Pharmaceuticals, Inc. |
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| Substance Name | ESOMEPRAZOLE MAGNESIUM; NAPROXEN |
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| Strength | 20; 375 |
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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], Cytochrome P450 2C19 Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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