Germany· DE-A57-bfc890d31d7a5b49
Flucinar
A medicinal product containing fluocinolone acetonide, registered in Germany by Abanta Pharma Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Fluocinolone Acetonide
- Manufacturer
- Abanta Pharma Gmbh
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fluocinolone acetonide in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesDerma-Smoothe/FSRoyal Pharmaceuticals, LLC
- PolandFlucinarPharmaVitae Sp. z o.o. sp. k.
- United KingdomILUVIEN 190microgram intravitreal implant in applicatorAlimera Sciences Ltd
- NorwayIluvienAlimera
- FinlandIluvienAbacus Medicine A/S
- Japanフルオシノロンアセトニド田辺ファーマ
- CanadaDERMA SMOOTHE/FS LIQ 0.01%HILL DERMACEUTICALS INC
- CzechiaFLUCINARBausch Health Ireland Limited, Dublin
Authorised across Europe · EMA
The same active substance is authorised in 23 EEA countries. Names it is sold under:
- Austria · Iluvien
- Belgium · Iluvien
- Bulgaria · Абрикорт, Флуцинар
- Czechia · Flucinar, Iluvien
- Denmark · Iluvien, Otazem
- Spain · Ekzem, Fluocid Forte
- Finland · Iluvien, Otazem
- France · Iluvien
- United Kingdom (Northern Ireland) · Iluvien, Synalar
- Greece · Synalar Simple
- Hungary · Flucinar
- Ireland · Iluvien
- Italy · Ekzem, Fluovitef
- Lithuania · Flucinar
- Luxembourg · Iluvien
- Latvia · Flucinar
- Netherlands · Iluvien
- Norway · Iluvien, Otazem
- Poland · Flucinar, Iluvien
- Portugal · Ekzem, Iluvien
- Romania · Fluocinolon Acetonid Laropharm
- Sweden · Iluvien, Otazem
- Slovakia · Flucinar
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of EMA Article 57 (European Union). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/eff7112e-3bde-41dd-8d2f-8e526a6747ad GET /v1/drugs/eff7112e-3bde-41dd-8d2f-8e526a6747ad?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"pzn": null,
"route": "Cutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Fluocinolone Acetonide",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about fluocinolone acetonide.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.