United Kingdom· GB-APID-15417811000001100
FML Liquifilm 0.1% ophthalmic suspension
A medicinal product containing fluorometholone, registered in United Kingdom by Waymade Healthcare Plc.
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
- Waymade Healthcare Plc
- 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 · 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
Fluorometholone in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesFlarexEyevance Pharmaceuticals
- PolandFlarexDelfarma 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/23d1d5bd-0e68-49cb-b6a5-1106e664cf8e GET /v1/drugs/23d1d5bd-0e68-49cb-b6a5-1106e664cf8e?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": "15417811000001100",
"desc": "FML Liquifilm 0.1% ophthalmic suspension (Waymade Healthcare Plc)",
"form": "Eye drops",
"vpid": "42189711000001101",
"source": "dmd",
"vtm_id": "776000006",
"strength": "1 mg",
"substance": "Fluorometholone",
"ingredient": "Fluorometholone",
"supplier_code": "2091401000001103"
}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.