Hydrochlorothiazide

Product NDC

68788-9920

11-digit product format

687889920

Labeler code

68788

Product ID

68788-9920_f46deca7-c260-4767-812a-84086bddf8a4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA040412

Marketing category

ANDA

Marketing start

2012-01-30

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

2019-12-31

Current FDA listing

Historical FDA.report record