NDC Code | 85722-0002-4 |
Package Description | 118 mL in 1 BOTTLE (85722-0002-4) |
Product NDC | 85722-0002 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Dextromethorphan Hydrobromide And Guaifenesin |
Non-Proprietary Name | Dextromethorphan Hydrobromide And Guaifenesin |
Dosage Form | SYRUP |
Usage | ORAL |
Start Marketing Date | 20210201 |
Marketing Category Name | OTC MONOGRAPH DRUG |
Application Number | M012 |
Manufacturer | KJD Pharma Private Limited |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength | 20; 300 |
Strength Unit | mg/5mL; mg/5mL |
Pharmacy Classes | 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] |