FDA
approval
· 2022-03-28
FDA Approved: CAPRELSA — Supplemental Application (Genzyme Corporation)
Summary
The FDA approved a supplemental application for CAPRELSA (vandetanib) submitted by Genzyme Corporation.
Upgrade for the full analysis, importance score, and drug timeline.
Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for CAPRELSA (VANDETANIB)