"11822-2219-1" National Drug Code (NDC)

NDC Code	11822-2219-1
Package Description	1 BOTTLE in 1 CARTON (11822-2219-1) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product NDC	11822-2219
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Relief Dm
Non-Proprietary Name	Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20230315
Marketing Category Name	ANDA
Application Number	ANDA207602
Manufacturer	Rite Aid Corporation
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]