← FDA DRUG APPROVALS

FDA NDA · NDA050697

BIAXIN XL

Sponsor: ABBVIE INC

APPLICATION
NDA050697
TYPE
NDA
ORIGINAL APPROVAL
1993-12-23
LATEST ACTION
2004-07-19
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

BIAXIN XLDiscontinued
CLARITHROMYCIN 250MG · TABLET · ORAL
BIAXIN XLDiscontinued
CLARITHROMYCIN 500MG · TABLET · ORAL

Approval history

2004-07-19Labeling · Supplement 3 · standardLetterAP
2002-05-24Efficacy · Supplement 2 · standardAP
1993-12-23Type 6 - New Indication (no longer used) · Original · standardAP
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 →