"66689-345-99" National Drug Code (NDC)

NDC Code	66689-345-99
Package Description	100 TABLET in 1 BOTTLE (66689-345-99)
Product NDC	66689-345
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Chlorthalidone
Non-Proprietary Name	Chlorthalidone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190624
End Marketing Date	20230531
Marketing Category Name	ANDA
Application Number	ANDA211063
Manufacturer	VistaPharm, Inc.
Substance Name	CHLORTHALIDONE
Strength	25
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis [PE], Thiazide-like Diuretic [EPC]