Hydrochlorothiazide

Product NDC

0615-1562

11-digit product format

006151562

Labeler code

0615

Product ID

0615-1562_e4155f64-58c6-43d2-a944-cad2b13e78ae

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA040412

Marketing category

ANDA

Marketing start

2002-03-29

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

50 mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record