| NDC Code | 51316-549-06 |
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| Package Description | 1 POWDER, FOR SOLUTION in 1 PACKET (51316-549-06) |
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| Product NDC | 51316-549 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Theraflu Relief Max Strength |
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| Proprietary Name Suffix | Nighttime |
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| Non-Proprietary Name | Acetaminophen, Chlorpheniramine Maleate And Dextromethophan Hbr |
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| Dosage Form | POWDER, FOR SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20230417 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | CVS PHARMACY |
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| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
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| Strength | 1000; 4; 30 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
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