"57237-002-01" National Drug Code (NDC)

NDC Code	57237-002-01
Package Description	100 CAPSULE in 1 BOTTLE (57237-002-01)
Product NDC	57237-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Hydrochlorothiazide
Non-Proprietary Name	Hydrochlorothiazide
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20070919
Marketing Category Name	ANDA
Application Number	ANDA078164
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	HYDROCHLOROTHIAZIDE
Strength	12.5
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]