Hydrochlorothiazide

Product NDC

0143-3125

11-digit product format

001433125

Labeler code

0143

Product ID

0143-3125_e77821f2-101f-4189-873c-ed9065083bb9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrochlorothiazide

Dosage form

CAPSULE

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA077885

Marketing category

ANDA

Marketing start

2007-11-26

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record