FDA
approval
· 2018-12-11
FDA Approved: ZEVALIN — Supplemental Application (Acrotech Biopharma Inc)
Summary
The FDA approved a supplemental application for ZEVALIN (ibritumomab tiuxetan) submitted by Acrotech Biopharma Inc.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for ZEVALIN (IBRITUMOMAB TIUXETAN)