"50090-1078-0" National Drug Code (NDC)

NDC Code	50090-1078-0
Package Description	2 BLISTER PACK in 1 CARTON (50090-1078-0) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	50090-1078
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucinex Dm
Non-Proprietary Name	Guaifenesin And Dextromethorphan Hydrobromide
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20120626
Marketing Category Name	NDA
Application Number	NDA021620
Manufacturer	A-S Medication Solutions
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength	30; 600
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]