JUN 2, 2026 · REGULATORY LABEL UPDATE
FDA supplemental approval: Saxenda (Labeling)
U.S. Food and Drug Administration
FDA supplemental approval for labeling change to liraglutide (Saxenda); describes regulatory action only, not clinical trial evidence or efficacy data.
Reported
Approval date2026-06-02
Product strengthLIRAGLUTIDE 18MG/3ML (6MG/ML)