← FDA DRUG APPROVALS

FDA ANDA · ANDA209613

TERIFLUNOMIDE

Sponsor: AMNEAL PHARMS CO

APPLICATION
ANDA209613
TYPE
ANDA
ORIGINAL APPROVAL
2018-09-28
LATEST ACTION
2025-03-26
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

TERIFLUNOMIDEDiscontinued
TERIFLUNOMIDE 14MG · TABLET · ORAL
TERIFLUNOMIDEDiscontinued
TERIFLUNOMIDE 7MG · TABLET · ORAL

Approval history

2025-03-26Labeling · Supplement 10 · standardAP
2025-03-26Labeling · Supplement 9 · standardAP
2024-02-20Labeling · Supplement 7 · standardAP
2020-11-05Labeling · Supplement 3 · standardAP
2019-11-29Labeling · Supplement 1 · standardAP
2018-09-28UNKNOWN · 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 →