Ireland· IE-PA-PA1824/008/001
FML 0.1% w/v Eye Drops Suspension
A fluorometholone product containing fluorometholone, registered in Ireland by AbbVie Limited. The same ATC class is registered in 10 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Fluorometholone is registered in 10 of 19 countries.
Countries holding a registration under ATC S01BA07 (fluorometholone), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 7 of them publish a price we can compare per daily dose
Fluorometholone · ATC S01BA07
10 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Finlandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Statesprice
The record
At a glance
HPRA (Ireland)- Active substance
- Fluorometholone
- Manufacturer
- AbbVie Limited
- Country
- Ireland (IE)
- ATC code
- S01BA07
- ATC class
- Fluorometholone
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA1824/008/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
55 interactions on record for fluorometholone.
Graded by severity as the source publishes them — 41 moderate. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Fluorometholone · interactions on record
55 records
- 41 moderate
- 14 info
Most severe, free to view
- MiconazoleA07AC01moderate
- LonafarnibA16AX20moderate
- VoxelotorB06AX03moderate
- ConivaptanC03XA02moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
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
- United KingdomFML Liquifilm 0.1% ophthalmic suspensionDE Pharmaceuticals
- PolandFlarexInPharm Sp. z o.o.
- BelgiumFlarex 1 mg/mlNovartis Pharma
- NorwayEfflumidexAbbvie AS
- CzechiaEFFLUMIDEX LIQUIFILMAbbVie s.r.o., Praha
- FinlandFML LIQUIFILMAbbVie Oy
- SpainFML 1 mg/ml colirio en suspensiónAbbvie Spain, S.L.U.
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
- United Kingdom (Northern Ireland) · Fml Liquifilm Ophthalmic
- Greece · Flucon, Fml
- Hungary · Efflumidex Liquifilm, Flucon
- 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 HPRA (Ireland). 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/e803a84e-fb24-4665-b4cb-e324a2b3a975 GET /v1/drugs/e803a84e-fb24-4665-b4cb-e324a2b3a975?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.
{
"form": "Eye drops, suspension",
"routes": [
"Topical use"
],
"source": "hpra",
"atc_all": [
"S01BA",
"S01BA07"
],
"strength": null,
"pa_number": "PA1824/008/001",
"substances": [
"Fluorometholone"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Not marketed",
"authorised_at": "01/04/1978",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}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.