"37808-830-20" National Drug Code (NDC)

NDC Code	37808-830-20
Package Description	1 BOTTLE, PLASTIC in 1 BOX (37808-830-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product NDC	37808-830
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Relief
Non-Proprietary Name	Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20230605
Marketing Category Name	ANDA
Application Number	ANDA207342
Manufacturer	H E B
Substance Name	GUAIFENESIN
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]