"71179-002-21" National Drug Code (NDC)

NDC Code	71179-002-21
Package Description	3 BLISTER PACK in 1 CARTON (71179-002-21) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	71179-002
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Guaifenesin
Non-Proprietary Name	Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20220627
Marketing Category Name	ANDA
Application Number	ANDA210453
Manufacturer	VESPYR BRANDS, INC.
Substance Name	GUAIFENESIN
Strength	1200
Strength Unit	mg/1
Pharmacy Classes	Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]