| NDC Code | 50580-232-01 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (50580-232-01) / 10 TABLET, CHEWABLE in 1 BLISTER PACK |
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| Product NDC | 50580-232 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Childrens Benadryl Chewables |
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| Non-Proprietary Name | Diphenhydramine Hydrochloride |
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| Dosage Form | TABLET, CHEWABLE |
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| Usage | ORAL |
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| Start Marketing Date | 20160711 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | Johnson & Johnson Consumer Inc. |
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| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 12.5 |
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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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