🏅 FDA Orphan Designation
Retisert
Fluocinolone
Manufacturer: Bausch & Lomb Pharmaceuticals, Inc.
FDA-Approved Indications (2)
Rare genetic disorder of the posterior segment of the eyeOrphan Designation
Treatment of chronic non-infectious uveitis affecting the posterior segment of the eye
RETISERT is indicated for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye
Population: all ages
Indications & Usage
1 INDICATIONS AND USAGE RETISERT ® is indicated for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye. RETISERT is a corticosteroid indicated for the treatment of chronic noninfectious uveitis affecting the posterior segment of the eye. (1)
💙 Support Programs
View all →Retisert
Bausch and Lomb
Retisert
Bausch & Lomb Pharmaceuticals, Inc.
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Medical disclaimer: This information is for educational purposes only. Always consult a qualified healthcare provider before making treatment decisions. Data sourced from FDA and current as of our last update.