Iceland· IS-980195 (IS)
Xalatan
A latanoprost product containing latanoprostum inn, registered in Iceland by Viatris ApS. The same ATC class is registered in 18 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Latanoprost is registered in 18 of 19 countries.
Countries holding a registration under ATC S01EE01 (latanoprost), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 10 of them publish a price we can compare per daily dose
Latanoprost · ATC S01EE01
18 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Italyprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Sweden
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Latanoprostum INN
- Manufacturer
- Viatris ApS
- Country
- Iceland (IS)
- ATC code
- S01EE01
- ATC class
- Latanoprost
- Defined daily dose
- 0.1 ml, AT
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 8, 2026
Packs & prices · 2
2 priced- ean0490912,5 ml x3 glösISK 8521
- ean5831052,5 ml x1 glasISK 4168
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
173 interactions on record for latanoprost.
Graded by severity as the source publishes them — 173 info. 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
Latanoprost · interactions on record
173 records
Same medicine, other countries
Latanoprost in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaAKISTANPharmaselect International Beteiligungs GmbH, Vídeň
- SpainARULATAN 50 microgramos/ml COLIRIO EN SOLUCIONDr. Gerhard Mann Chem.-Pharm. Fabrik Gmbh
- United KingdomCatiolanze 50micrograms/ml eye drops emulsion 0.3ml unit doseSanten UK Ltd
- SwedenAkistan 50 mikrogram/ml Ögondroppar, lösningPharmaselect International Beteiligungs GmbH
- ItalyDROPLATANOMNIVISION ITALIA S.R.L.
- BelgiumCatiolanze 50 µg/mlSanten
- SwitzerlandCatiolanze
- United StatesIYUZEHThea Pharma Inc.
Authorised across Europe · EMA
The same active substance is authorised in 30 EEA countries. Names it is sold under:
- Austria · Akistan, Latacris
- Belgium · Latanea, Latanoprost Eg
- Bulgaria · Akistan, Ксалатан
- Cyprus · Gisolom, Latanoprost Demo
- Czechia · Akistan, Latanoprost Olikla
- Germany · Akistan, Latanelb
- Denmark · Latanoprost Genetic, Latanoprost Rivopharm
- Estonia · Glaumax, Latanoprost Actavis
- Spain · Latanest, Latanoprost Aurovitas
- Finland · Latanoprost Sandoz, Latanoprost Stada
- France · Latanoprost Bgr, Latanoprost Biogaran
- United Kingdom (Northern Ireland) · Latanoprost, Latanoprost Accord
- Greece · Latandrops, Lataneau
- Croatia · Lapovis, Latanox
- Hungary · Akistan, Laprosep
- Ireland · Latanoprost Genetic, Loravis
- Italy · Droplatan, Galaxia
- Liechtenstein · Catiolanze
- Lithuania · Latanoprost Actavis, Latanoprost Elvim
- Luxembourg · Latanea, Latanoprost Eg
- Latvia · Latanoprost Actavis, Latanoprost Elvim
- Malta · Latanoprost Genetic, Lunaris
- Netherlands · Latanea, Latanmono Conserveermiddelvrij
- Norway · Catiolanze, Ditiamgo
- Poland · Akistan, Latanoprost Genoptim
- Portugal · Enicil, Enicilfree
- Romania · Akistan, Glautan
- Sweden · Latanoprost Actavis, Latanoprost Genetic
- Slovenia · Akistan, Latanoprost Genetic
- Slovakia · Akistan, Latanoprost Olikla
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 Icelandic Medicines Agency (Iceland). 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/f10adc45-846a-4c95-93f0-a46058b991b1 GET /v1/drugs/f10adc45-846a-4c95-93f0-a46058b991b1?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": "Augndropar, lausn",
"source": "lyfjastofnun",
"atc_raw": "S01EE01",
"marketed": true,
"strength": "50 míkróg/ml",
"ma_number": "980195 (IS)",
"substance": "Latanoprostum INN",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "36350"
}See everything about latanoprost.
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.