NDC Code | 69367-184-08 |
Package Description | 240 mL in 1 BOTTLE (69367-184-08) |
Product NDC | 69367-184 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride |
Non-Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride |
Dosage Form | LIQUID |
Usage | ORAL |
Start Marketing Date | 20180315 |
Marketing Category Name | OTC MONOGRAPH DRUG |
Application Number | M012 |
Manufacturer | Westminster Pharmaceuticals, LLC |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength | 18; 200; 10 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
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] |