| NDC Code | 21130-814-05 |
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| Package Description | 50 TABLET in 1 BOTTLE (21130-814-05) |
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| Product NDC | 21130-814 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Naproxen Sodium Diphenhydramine Hydrochloride |
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| Non-Proprietary Name | Naproxen Sodium Diphenhydramine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20230630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213663 |
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| Manufacturer | SAFEWAY |
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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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