"30142-701-20" National Drug Code (NDC)

NDC Code	30142-701-20
Package Description	1 BLISTER PACK in 1 CARTON (30142-701-20) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	30142-701
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus
Non-Proprietary Name	Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20170907
Marketing Category Name	NDA
Application Number	NDA021282
Manufacturer	KROGER COMPANY
Substance Name	GUAIFENESIN
Strength	600
Strength Unit	mg/1