"42507-222-20" National Drug Code (NDC)

NDC Code	42507-222-20
Package Description	1 BOTTLE in 1 CARTON (42507-222-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (42507-222-01)
Product NDC	42507-222
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Dm
Non-Proprietary Name	Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20260225
Marketing Category Name	ANDA
Application Number	ANDA207602
Manufacturer	HyVee Inc
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]