Iceland· IS-EU/1/14/914/001
Vimizim
A elosulfase alfa product containing elosulfasum alfa inn, registered in Iceland by BioMarin International Limited. The same ATC class is registered in 14 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Elosulfase alfa is registered in 14 of 19 countries.
Countries holding a registration under ATC A16AB12 (elosulfase alfa), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 9 of them publish a price we can compare per daily dose
Elosulfase alfa · ATC A16AB12
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Elosulfasum alfa INN
- Manufacturer
- BioMarin International Limited
- Country
- Iceland (IS)
- ATC code
- A16AB12
- ATC class
- Elosulfase alfa
- Defined daily dose
- 20 mg, P
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 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
Elosulfase alfa in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NorwayVimizimOrifarm AS
- SwitzerlandVimizim 5mg/5ml, Konzentrat zur Herstellung einer InfusionslösungDRAC AG
- CzechiaVIMIZIMBioMarin International Limited, Dublin
- FinlandVimizimBiomarin International Limited
- IrelandVimizim 1 mg/ml concentrate for solution for infusionBiomarin International Limited
- PolandVimizimBioMarin International Ltd.
- SwedenVimizim 1 mg/ml Koncentrat till infusionsvätska, lösningBioMarin International Limited
- BelgiumVimizim 1 mg/mlBioMarin International
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Liechtenstein · Vimizim
- Norway · Vimizim
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/0b14c417-fbd7-4dbb-a1fb-ecd55b7c5599 GET /v1/drugs/0b14c417-fbd7-4dbb-a1fb-ecd55b7c5599?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": "Innrennslisþykkni, lausn",
"source": "lyfjastofnun",
"atc_raw": "A16AB12",
"marketed": false,
"strength": "1 mg/ml",
"ma_number": "EU/1/14/914/001",
"substance": "Elosulfasum alfa INN",
"other_info": "Markaðssetning á Íslandi er háð því að Lyfjastofnun hafi staðfest að sérstök skilyrði er varða öryggi og verkun við notkun lyfsins séu uppfyllt.",
"legal_status": "(R) Lyfseðilsskylt\r\n(H) Sjúkrahúsmerkt",
"ma_issued_serial": "41757"
}See everything about elosulfase alfa.
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.