Hydrochlorothiazide

Product NDC

0179-0065

11-digit product format

001790065

Labeler code

0179

Product ID

0179-0065_7bc0ec6d-ffb1-6486-e053-2a91aa0addd3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA040907

Marketing category

ANDA

Marketing start

2010-06-07

Marketing end

2020-09-30

Substance

HYDROCHLOROTHIAZIDE

Active strength

25 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record