FDA
label_change
· 2024-01-23
FDA Approved: VABRINTY — Supplemental Application (URONOVA PHARMACEUTICALS, INC.)
Summary
FDA approved a supplemental application for VABRINTY (leuprolide acetate) from Uronova Pharmaceuticals to modify the drug's labeling.
Upgrade for the full analysis, importance score, and drug timeline.
Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for VABRINTY (LEUPROLIDE ACETATE)