"57237-359-12" National Drug Code (NDC)

NDC Code	57237-359-12
Package Description	118 mL in 1 BOTTLE (57237-359-12)
Product NDC	57237-359
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucolyte
Non-Proprietary Name	Guaifenesin
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20251222
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M012
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	GUAIFENESIN
Strength	100
Strength Unit	mg/5mL
Pharmacy Classes	Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]