Retisert FDA Approval History
FDA Approved: Yes (First approved April 8, 2005)
Brand name: Retisert
Generic name: fluocinolone acetonide
Dosage form: Intravitreal Implant
Company: Bausch & Lomb Inc.
Treatment for: Uveitis
Retisert (fluocinolone acetonide) intravitreal implant is indicated for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye.
Development timeline for Retisert
| Date | Article |
|---|---|
| Apr 8, 2005 | Approval Retisert Bausch & Lomb - Treatment for Chronic Non-Infectious Uveitis |
Further information
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