| NDC Code | 63868-411-20 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (63868-411-20) / 20 TABLET in 1 BOTTLE, PLASTIC |
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| Product NDC | 63868-411 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Naproxen Pm |
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| Non-Proprietary Name | Naproxen Sodium |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20190131 |
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| End Marketing Date | 20250601 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209726 |
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| Manufacturer | QUALITY CHOICE (Chain Drug Marketing Association) |
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| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM |
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| Strength | 25; 220 |
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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], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC] |
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