Belgium· BE-AMP-SAM663232-00
Piasky 340 mg
A crovalimab product containing crovalimab, registered in Belgium by Roche Registration. The same ATC class is registered in 11 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) 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: Belgium, from FAMHP / AFMPS (Belgium)
- 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
FAMHP / AFMPS (Belgium)- Active substance
- Crovalimab
- Manufacturer
- Roche Registration
- Country
- Belgium (BE)
- ATC code
- L04AJ07
- ATC class
- Crovalimab
- Defined daily dose
- 24.3 mg, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb4866901
- be_apb7743362
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.
- CzechiaPIASKYRoche Registration GmbH, Grenzach-Wyhlen
- SpainPIASKY 340 MG SOLUCION INYECTABLE Y PARA PERFUSIONRoche Registration Gmbh
- IcelandPiaskyRoche Registration GmbH*
- PolandPiaskyRoche 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 FAMHP / AFMPS (Belgium). 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/e84c42d8-c434-45ef-a56f-65c230f1109c GET /v1/drugs/e84c42d8-c434-45ef-a56f-65c230f1109c?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": "Solution for injection/infusion",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Piasky 340 mg",
"name_fr": "Piasky 340 mg",
"name_nl": "Piasky 340 mg",
"amp_code": "SAM663232-00",
"strengths": [
"170.0000",
"170.0000"
],
"pack_count": 1,
"substances": [
"Crovalimab"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Crovalimab",
"authorisation_numbers": [
"EU/1/24/1848/001"
]
}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.