"70000-0129-1" National Drug Code (NDC)

NDC Code	70000-0129-1
Package Description	180 mL in 1 BOTTLE (70000-0129-1)
Product NDC	70000-0129
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Maximum Strength Mucus Relief Dm
Non-Proprietary Name	Dextromethorphan Hydrobromide And Guaifenesin
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20170306
Marketing Category Name	OTC MONOGRAPH FINAL
Application Number	part341
Manufacturer	CARDINAL HEALTH
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]