← FDA DRUG APPROVALS

FDA ANDA · ANDA071379

FUROSEMIDE

Sponsor: ANI PHARMS

APPLICATION
ANDA071379
TYPE
ANDA
ORIGINAL APPROVAL
1987-01-02
LATEST ACTION
2002-11-07
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

FUROSEMIDEDiscontinued
FUROSEMIDE 20MG · TABLET · ORAL

Approval history

2002-11-07Manufacturing (CMC) · Supplement 20AP
2001-08-31Manufacturing (CMC) · Supplement 19AP
1999-11-10Manufacturing (CMC) · Supplement 18AP
1999-06-23Manufacturing (CMC) · Supplement 16AP
1998-12-11Labeling · Supplement 17AP
1996-04-29Labeling · Supplement 15AP
1993-06-11Labeling · Supplement 14AP
1993-04-08Labeling · Supplement 13AP
1992-08-24Labeling · Supplement 12AP
1992-06-02Labeling · Supplement 11AP
1990-12-04Labeling · Supplement 10AP
1990-08-02Labeling · Supplement 9AP
1990-05-08Manufacturing (CMC) · Supplement 6AP
1990-05-08Manufacturing (CMC) · Supplement 7AP
1990-04-12Labeling · Supplement 8AP
1988-11-04Manufacturing (CMC) · Supplement 5AP
1988-06-20Manufacturing (CMC) · Supplement 4AP
1988-06-20Manufacturing (CMC) · Supplement 2AP
1988-06-20Manufacturing (CMC) · Supplement 3AP
1987-09-10Manufacturing (CMC) · Supplement 1AP
1987-01-02OriginalAP
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 →