| NDC Code | 81033-009-51 |
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| Package Description | 100 CUP, UNIT-DOSE in 1 CASE (81033-009-51) / 10 mL in 1 CUP, UNIT-DOSE (81033-009-10) |
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| Product NDC | 81033-009 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diphenhydramine Hydrochloride |
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| Non-Proprietary Name | Diphenhydramine Hydrochloride |
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| Dosage Form | ELIXIR |
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| Usage | ORAL |
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| Start Marketing Date | 19820210 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA087513 |
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| Manufacturer | Kesin Pharma Corporation |
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| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 12.5 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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