"0113-2219-01" National Drug Code (NDC)

NDC Code	0113-2219-01
Package Description	1 BOTTLE in 1 CARTON (0113-2219-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product NDC	0113-2219
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Good Sense Mucus Dm
Non-Proprietary Name	Dextromethorphan Hydrobromide, Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20190710
Marketing Category Name	ANDA
Application Number	ANDA207602
Manufacturer	L. Perrigo Company
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]