Hydrochlorothiazide

Product NDC

67544-338

11-digit product format

675440338

Labeler code

67544

Product ID

67544-338_5d3ad7cd-d844-49b9-adde-a05f12d0ea8a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Aphena Pharma Solutions - Tennessee, LLC

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record