Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2015-03-30

FDA Approved: RETISERT — Supplemental Application (Bausch & Lomb Incorporated)

View source ↗

Summary

FDA approved a supplemental application for RETISERT (fluocinolone acetonide) submitted by Bausch & Lomb Incorporated, related to the corticosteroid intravitrea…

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

Diseases / indications

Drugs mentioned

  • Retisert (fluocinolone acetonide)

Snippet

SUPPL AP for RETISERT (FLUOCINOLONE ACETONIDE)