Finland· FI-REL-REL61750
Piasky
A crovalimab product containing crovalimab, registered in Finland by Roche Registration GmbH. The same ATC class is registered in 11 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Crovalimab is registered in 11 of 19 countries.
Countries holding a registration under ATC L04AJ07 (crovalimab), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 7 of them publish a price we can compare per daily dose
Crovalimab · ATC L04AJ07
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Fimea (Finland)- Active substance
- Crovalimab
- Manufacturer
- Roche Registration GmbH
- Country
- Finland (FI)
- ATC code
- L04AJ07
- ATC class
- Crovalimab
- Defined daily dose
- 24.3 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
Crovalimab in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumPiasky 340 mgRoche Registration
- SwitzerlandPiasky 340 mg/ 2 ml, Injektions-/InfusionslösungRoche Pharma (Schweiz) AG
- CzechiaPIASKYRoche Registration GmbH, Grenzach-Wyhlen
- SpainPIASKY 340 MG SOLUCION INYECTABLE Y PARA PERFUSIONRoche Registration Gmbh
- United KingdomPiaSky 340mg/2ml solution for injection vialsRoche Products Ltd
- IrelandPiaskyRoche Registration GmbH
- IcelandPiaskyRoche Registration GmbH*
- Japanクロバリマブ(遺伝子組換え)中外製薬
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Piasky
- Liechtenstein · Piasky
- Norway · Piasky
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/de8a82ab-21fd-41a5-9a52-5496ed83b4ef GET /v1/drugs/de8a82ab-21fd-41a5-9a52-5496ed83b4ef?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": "24.3",
"form": "injektio-/infuusioneste, liuos",
"route": "Ihon alle",
"ddd_unit": "mg",
"strength": "340 mg",
"atc_label": "krovalimabi",
"ma_number": null,
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": "EU/1/24/1848/001",
"fimea_rel_id": "REL61750",
"authorised_at": "2024-08-22"
}See everything about crovalimab.
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.