"69256-834-14" National Drug Code (NDC)

NDC Code	69256-834-14
Package Description	14 BLISTER PACK in 1 CARTON (69256-834-14) > 1 TABLET in 1 BLISTER PACK
Product NDC	69256-834
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Relief Dm
Proprietary Name Suffix	Maximum Strength
Non-Proprietary Name	Guaifenesin, Dextromethorphan Hbr
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20210528
Marketing Category Name	ANDA
Application Number	ANDA209692
Manufacturer	Harris Teeter, LLC
Substance Name	DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength	60; 1200
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]