| NDC Code | 50269-226-54 |
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| Package Description | 25 TABLET, FILM COATED in 1 BOX (50269-226-54) |
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| Product NDC | 50269-226 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Benadryl Ultra Tab |
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| Non-Proprietary Name | Diphenhydramine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20180816 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | JC World Bell Wholesale Co., Inc. |
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| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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