"72036-012-20" National Drug Code (NDC)

NDC Code	72036-012-20
Package Description	2 BLISTER PACK in 1 CARTON (72036-012-20) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	72036-012
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Relief Dm
Non-Proprietary Name	Guaifenesin And Dextromethorphan Hbr
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20240816
Marketing Category Name	ANDA
Application Number	ANDA206941
Manufacturer	Harris Teeter
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]