NDC Code | 83324-137-14 |
Package Description | 14 BLISTER PACK in 1 CARTON (83324-137-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 83324-137 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Mucus Relief Dm |
Non-Proprietary Name | Guaifenesin Dextromethorphan Hbr |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20240731 |
Marketing Category Name | ANDA |
Application Number | ANDA209692 |
Manufacturer | QUALITY CHOICE (Chain Drug Marketing Association) |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength | 60; 1200 |
Strength Unit | mg/1; mg/1 |
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] |