← FDA DRUG APPROVALS

FDA ANDA · ANDA087082

CHLORTHALIDONE

Sponsor: WATSON LABS

APPLICATION
ANDA087082
TYPE
ANDA
ORIGINAL APPROVAL
1981-08-25
LATEST ACTION
1989-03-01
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CHLORTHALIDONEDiscontinued
CHLORTHALIDONE 50MG · TABLET · ORAL

Approval history

1989-03-01Labeling · Supplement 22AP
1988-10-14Labeling · Supplement 21AP
1988-06-07Labeling · Supplement 20AP
1981-08-25OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industryGMP disciplineFDA drug shortagesFDA enforcement & recalls

Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →