This brand name is authorized in United States. It is also authorized in Austria, Finland, France, Ireland, Netherlands, New Zealand, Poland, Spain, UK.
The drug ILUVIEN contains one active pharmaceutical ingredient (API):
1
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UNII
0CD5FD6S2M - FLUOCINOLONE ACETONIDE
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Fluocinolone acetonide is a synthetic fluorinated corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictive properties. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| ILUVIEN Intravitreal implant | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| S01BA15 | Fluocinolone acetonide | S Sensory organs → S01 Ophthalmologicals → S01B Antiinflammatory agents → S01BA Corticosteroids, plain |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| ES | Centro de información online de medicamentos de la AEMPS | 76832 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 506248 |
| FR | Base de données publique des médicaments | 61412157 |
| GB | Medicines & Healthcare Products Regulatory Agency | 225161 |
| NL | Z-Index G-Standaard, PRK | 204315 |
| NZ | Medicines and Medical Devices Safety Authority | 21705 |
| PL | Rejestru Produktów Leczniczych | 100333342 |
| US | FDA, National Drug Code | 68611-190 |
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