Hydrochlorothiazide

Product NDC

0440-7595

11-digit product format

004407595

Labeler code

0440

Product ID

0440-7595_21e2282c-24ff-4c8c-a830-df006c89e914

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Liberty Pharmaceuticals, Inc.

Application

ANDA040412

Marketing category

ANDA

Marketing start

2002-03-29

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

25 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record