United Kingdom· GB-APID-3149611000001105
FML Liquifilm 0.1% ophthalmic suspension
A medicinal product containing fluorometholone, registered in United Kingdom by AbbVie Ltd.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Fluorometholone
- Manufacturer
- AbbVie Ltd
- Country
- United Kingdom (GB)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 4
- gtin5016007070705
- gtin05016007070705
- gtin5016007070804
- gtin05016007070804
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fluorometholone in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesFlarexHarrow Eye, LLC
- PolandFlarexInPharm Sp. z o.o.
- BelgiumFlarex 1 mg/mlNovartis Pharma
- NorwayEfflumidexAbbvie AS
- CzechiaEFFLUMIDEX LIQUIFILMAbbVie s.r.o., Praha
- FinlandFML LIQUIFILMOrifarm Oy
- SpainFML 1 mg/ml colirio en suspensiónAbbvie Spain, S.L.U.
- CanadaFMLABBVIE CORPORATION
Authorised across Europe · EMA
The same active substance is authorised in 19 EEA countries. Names it is sold under:
- Belgium · Fml
- Bulgaria · Фларекс
- Czechia · Efflumidex Liquifilm, Flarex
- Germany · Efflumidex, Fluoropos
- Spain · Fml, Isopto Flucon
- Finland · Fml Liquifilm
- France · Flucon
- Greece · Flucon, Fml
- Hungary · Efflumidex Liquifilm, Flucon
- Ireland · Fml
- Italy · Flarex, Fluaton
- Lithuania · Flarex
- Luxembourg · Fml
- Netherlands · Fml Liquifilm
- Poland · Flarex, Flucon
- Portugal · Fml - Liquifilm
- Romania · Flumetol S
- Slovenia · Flarex
- Slovakia · Efflumidex Liquifilm
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 NHS dm+d (United Kingdom). 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/d643a83e-701a-4c2c-bb6a-fbd5e6ebc625 GET /v1/drugs/d643a83e-701a-4c2c-bb6a-fbd5e6ebc625?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.
{
"apid": "3149611000001105",
"desc": "FML Liquifilm 0.1% ophthalmic suspension (AbbVie Ltd)",
"form": "Eye drops",
"vpid": "42189711000001101",
"source": "dmd",
"vtm_id": "776000006",
"strength": "1 mg",
"substance": "Fluorometholone",
"ingredient": "Fluorometholone",
"supplier_code": "20741511000001103"
}See everything about fluorometholone.
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.