"43598-008-01" National Drug Code (NDC)

NDC Code	43598-008-01
Package Description	5 BLISTER PACK in 1 CARTON (43598-008-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-008-20)
Product NDC	43598-008
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Guaifenesin 600 Mg
Non-Proprietary Name	Guaifenesin
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20220315
Marketing Category Name	ANDA
Application Number	ANDA215932
Manufacturer	Dr. Reddy's Laboratories Inc.
Substance Name	GUAIFENESIN
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]