"0121-0638-04" National Drug Code (NDC)

NDC Code	0121-0638-04
Package Description	118 mL in 1 BOTTLE (0121-0638-04)
Product NDC	0121-0638
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Guaifenesin Dm
Non-Proprietary Name	Guaifenesin And Dextromethorphan
Dosage Form	SYRUP
Usage	ORAL
Start Marketing Date	19920701
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	PAI Holdings, LLC
Substance Name	DEXTROMETHORPHAN; GUAIFENESIN
Strength	10; 100
Strength Unit	mg/5mL; mg/5mL
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]