| NDC Code | 68210-0099-3 |
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| Package Description | 1 BOTTLE in 1 CARTON (68210-0099-3) / 50 TABLET in 1 BOTTLE |
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| Product NDC | 68210-0099 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Extra Strength Pain Relief Pm |
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| Non-Proprietary Name | Acetaminophen And Diphenhydramine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20180410 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M013 |
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| Manufacturer | Spirit Pharmaceutical 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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