Hydrochlorothiazide

Product NDC

55289-136

11-digit product format

552890136

Labeler code

55289

Product ID

55289-136_7b1f80eb-f36b-5be4-e053-2a91aa0aac7d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA084878

Marketing category

ANDA

Marketing start

2006-08-01

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