| NDC Code | 17714-023-50 |
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| Package Description | 50 TABLET in 1 BOTTLE (17714-023-50) |
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| Product NDC | 17714-023 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Diphenhydramine Hydrochloride |
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| Non-Proprietary Name | Diphenhydramine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20120901 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Advance Pharmaceutical Inc. |
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| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 50 |
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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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