"59726-833-20" National Drug Code (NDC)

NDC Code	59726-833-20
Package Description	20 BLISTER PACK in 1 CARTON (59726-833-20) / 1 TABLET in 1 BLISTER PACK
Product NDC	59726-833
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Dm Extended Release
Non-Proprietary Name	Dextromethorphan Hydrobromide And Guaifenesin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190101
End Marketing Date	20260201
Marketing Category Name	ANDA
Application Number	ANDA209692
Manufacturer	P & L Development, LLC
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]