FDA.reportPublic FDA data

fluocinolone acetonide 0.18 MG Intravitreal Implant

RxCUI
2099361
RxNorm name
fluocinolone acetonide 0.18 MG Intravitreal Implant
Display name
fluocinolone acetonide 0.18 MG Intravitreal Implant
Full name
fluocinolone acetonide 0.18 MG Intravitreal Implant
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:27

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
YUTIQFLUOCINOLONE ACETONIDEANI Pharmaceuticals, Inc.f270cad8-ed82-4969-b785-831a1910bfa62026-02-19Warnings, Adverse reactionsExact identifier
rxcui: 2099361

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
f270cad8-ed82-4969-b785-831a1910bfa6fluocinolone acetonide 0.18 MG Intravitreal Implant [PSN] · fluocinolone acetonide 0.18 MG Drug Implant [SCD] · fluocinolone acetonide 0.18 MG Intravitreal Implant [SY]34These highlights do not include all the information needed to use YUTIQ ® safely and effectively. See full prescribing information for YUTIQ. YUTIQ ® (fluocinolone acetonide intravitreal implant) 0.18 mg, for intravitreal injection Initial U.S. Approval: 196320260219