"49035-839-06" National Drug Code (NDC)

NDC Code	49035-839-06
Package Description	180 mL in 1 BOTTLE (49035-839-06)
Product NDC	49035-839
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Maximum Strength Mucus Relief Dm
Non-Proprietary Name	Dextromethorphan Hydrobromide And Guaifenesin
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20180501
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	Wal-Mart Stores,Inc.,
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength	20; 400
Strength Unit	mg/20mL; mg/20mL
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]