| NDC Code | 69367-198-90 |
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| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (69367-198-90) |
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| Product NDC | 69367-198 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
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| Non-Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20181025 |
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| End Marketing Date | 20240401 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Westminster Pharmaceuticals, LLC |
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| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 17.5; 385; 10 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-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-1 Adrenergic Agonist [EPC] |
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