fluocinolone acetonide 0.19 MG Drug Implant [Iluvien]
- RxCUI
- 1552356
- RxNorm name
- fluocinolone acetonide 0.19 MG Drug Implant [Iluvien]
- Display name
- fluocinolone acetonide 0.19 MG Drug Implant [Iluvien]
- Full name
- fluocinolone acetonide 0.19 MG Drug Implant [Iluvien]
- Term type
- SBD
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:38:56
UNII Substances#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Iluvien | FLUOCINOLONE ACETONIDE | ANI Pharmaceuticals, Inc. | 4400e471-7402-11df-93f2-0800200c9a66 | 2026-01-28 | Warnings, Adverse reactions | 1552356 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm mappings | Terms | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 4400e471-7402-11df-93f2-0800200c9a66 | ILUVIEN 0.19 MG Intravitreal Drug Implant [PSN] · fluocinolone acetonide 0.19 MG Drug Implant [Iluvien] [SBD] · Iluvien 0.19 MG Drug Implant [SY] | 3 | 20 | These 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: 1963 | 20260128 |