"21130-500-58" National Drug Code (NDC)

NDC Code	21130-500-58
Package Description	1 BOTTLE in 1 CARTON (21130-500-58) > 40 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product NDC	21130-500
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Mucus Relief
Non-Proprietary Name	Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20130725
Marketing Category Name	ANDA
Application Number	ANDA078912
Manufacturer	Safeway
Substance Name	GUAIFENESIN
Strength	600
Strength Unit	mg/1