"37808-518-25" National Drug Code (NDC)

NDC Code	37808-518-25
Package Description	177 mL in 1 BOTTLE (37808-518-25)
Product NDC	37808-518
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Maximum Strength Dm Max
Non-Proprietary Name	Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20120914
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	H E B
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]