FDA.reportPublic FDA data

fluocinolone acetonide 0.19 MG Intravitreal Drug Implant

RxCUI
1552351
RxNorm name
fluocinolone acetonide 0.19 MG Intravitreal Drug Implant
Display name
fluocinolone acetonide 0.19 MG Intravitreal Drug Implant
Full name
fluocinolone acetonide 0.19 MG Intravitreal Drug Implant
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:38:56

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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
IluvienFLUOCINOLONE ACETONIDEANI Pharmaceuticals, Inc.4400e471-7402-11df-93f2-0800200c9a662026-01-28Warnings, Adverse reactionsExact identifier
rxcui: 1552351

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
4400e471-7402-11df-93f2-0800200c9a66fluocinolone acetonide 0.19 MG Intravitreal Drug Implant [PSN] · fluocinolone acetonide 0.19 MG Drug Implant [SCD]220These highlights do not include all the information needed to use ILUVIEN® safely and effectively. See full prescribing information for ILUVIEN. ILUVIEN® (fluocinolone acetonide intravitreal implant), 0.19 mg, for intravitreal use Initial U.S. Approval: 196320260128