Finland· FI-REL-REL57147
Evkeeza
A evinacumab product containing evinacumab, registered in Finland by Ultragenyx Germany GmbH. The same ATC class is registered in 12 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Evinacumab is registered in 12 of 19 countries.
Countries holding a registration under ATC C10AX17 (evinacumab), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 8 of them publish a price we can compare per daily dose
Evinacumab · ATC C10AX17
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
Fimea (Finland)- Active substance
- Evinacumab
- Manufacturer
- Ultragenyx Germany GmbH
- Country
- Finland (FI)
- ATC code
- C10AX17
- ATC class
- Evinacumab
- Defined daily dose
- 37.5 mg, P
- Reimbursed
- Not published by this register
- Source register
- Fimea (Finland)
- Last checked
- September 27, 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
Evinacumab in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumEvkeeza 150 mg/mlUltragenyx Germany
- CzechiaEVKEEZAUltragenyx Germany GmbH, Berlín
- United StatesEvkeezaRegeneron Pharmaceuticals, Inc.
- IcelandEvkeezaUltragenyx Germany GmbH
- NorwayEvkeezaUltragenyx Germany GmbH
- PolandEvkeezaUltragenyx Germany GmbH
- SwedenEvkeeza 150 mg/ml Koncentrat till infusionsvätska, lösningUltragenyx Germany GmbH
- IrelandEvkeeza 150 mg/ml concentrate for solution for infusionUltragenyx Germany GmbH
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Evkeeza
- Liechtenstein · Evkeeza
- Norway · Evkeeza
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 Fimea (Finland). 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/9656f237-f2e3-4e04-b241-1c3286e81b2f GET /v1/drugs/9656f237-f2e3-4e04-b241-1c3286e81b2f?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.
{
"ddd": null,
"form": "infuusiokonsentraatti, liuosta varten",
"route": "Laskimoon",
"ddd_unit": null,
"strength": "150 mg/ml",
"atc_label": "evinakumabi",
"ma_number": null,
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": "EU/1/21/1551/001-002",
"fimea_rel_id": "REL57147",
"authorised_at": "2021-06-17"
}See everything about evinacumab.
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.