| NDC Code | 59726-031-15 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (59726-031-15) / 150 TABLET, COATED in 1 BOTTLE, PLASTIC |
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| Product NDC | 59726-031 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Pain Reliever Pm |
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| Proprietary Name Suffix | Extra Strength |
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| Non-Proprietary Name | Acetaminophen, Diphenhydramine Hcl |
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| Dosage Form | TABLET, COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20150105 |
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| End Marketing Date | 20250105 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | P & L Development, LLC |
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| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 500; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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