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

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Summary

FDA approved a supplemental application for RETISERT, the fluocinolone acetonide implant by Bausch & Lomb. This action pertains to an amendment to the existing …

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Diseases / indications

• Noninfectious Posterior Uveitis
• Uveitis

Drugs mentioned

• Retisert (fluocinolone acetonide)

Snippet

SUPPL AP for RETISERT (FLUOCINOLONE ACETONIDE)