Chlorothiazide

Product NDC

0143-1210

11-digit product format

001431210

Labeler code

0143

Product ID

0143-1210_2af0405e-71c2-4074-bbd2-41ef19697dd0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA087736

Marketing category

ANDA

Marketing start

2005-08-30

Marketing end

0000-00-00

Substance

CHLOROTHIAZIDE

Active strength

500 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