| NDC Code | 50991-535-02 |
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| Package Description | 6 BLISTER PACK in 1 CARTON (50991-535-02) / 2 TABLET in 1 BLISTER PACK |
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| Product NDC | 50991-535 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Duraflu |
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| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Pseudoephedrine Hcl |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20151001 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M012 |
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| Manufacturer | Poly Pharmaceuticals, Inc. |
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| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 325; 20; 200; 60 |
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| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-Adrenergic Agonist [EPC] |
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