Poland· PL-100504822
Piasky
A crovalimab product containing crovalimabum, registered in Poland by Roche Registration GmbH. The same ATC class is registered in 11 of our 19 countries.
Checked against URPL (Poland) 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: Poland, from URPL (Poland)
- 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
URPL (Poland)- Active substance
- Crovalimabum
- Manufacturer
- Roche Registration GmbH
- Country
- Poland (PL)
- ATC code
- L04AJ07
- ATC class
- Crovalimab
- Defined daily dose
- 24.3 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin07613326085861
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
- CzechiaPIASKYRoche Registration GmbH, Grenzach-Wyhlen
- SpainPIASKY 340 MG SOLUCION INYECTABLE Y PARA PERFUSIONRoche Registration Gmbh
- IcelandPiaskyRoche Registration GmbH*
- SwitzerlandPiasky 340 mg/ 2 ml, Injektions-/InfusionslösungRoche Pharma (Schweiz) AG
- FinlandPiaskyRoche Registration GmbH
- United KingdomPiaSky 340mg/2ml solution for injection vialsRoche Products Ltd
- IrelandPiaskyRoche Registration GmbH
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 URPL (Poland). 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/ce741b97-0033-4d83-b4a3-91167822b9e1 GET /v1/drugs/ce741b97-0033-4d83-b4a3-91167822b9e1?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": "Roztwór do wstrzykiwań / do infuzji",
"source": "urpl",
"strength": "340 mg",
"packaging": "07613326085861 ¦ Rpz ¦ EU/1/24/1848/001 ¦ 157880\n1 fiol.",
"substance": "Crovalimabum 340 mg",
"common_name": "Crovalimabum",
"pl_product_id": "100504822",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}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.