| NDC Code | 0067-8136-10 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (0067-8136-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 0067-8136 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Theraflu Expressmax |
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| Proprietary Name Suffix | Daytime Severe Cold And Cough |
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| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160705 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | Haleon US Holdings LLC |
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| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 325; 10; 5 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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