Hydrochlorothiazide

Product NDC

69375-001

11-digit product format

693750001

Labeler code

69375

Product ID

69375-001_214338fb-33c0-44a5-8c2d-d43989bcfef8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

CAPSULE, GELATIN COATED

Route

ORAL

Labeler

Nationwide Pharmaceutical, LLC

Application

ANDA078391

Marketing category

ANDA

Marketing start

2015-03-01

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE

Active strength

13 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