Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2021-10-22

FDA Approved: CELLCEPT — Supplemental Application (Genentech, Inc.)

View source ↗

Summary

The FDA approved a supplemental application for Cellcept (mycophenolate mofetil hydrochloride) submitted by Genentech, Inc.

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • CELLCEPT (mycophenolate mofetil hydrochloride)

Snippet

SUPPL AP for CELLCEPT (MYCOPHENOLATE MOFETIL HYDROCHLORIDE)