Belgium· BE-AMP-SAM342185-00
Removab 10 µg
A catumaxomab product containing catumaxomab, registered in Belgium by Neovii Biotech. The same ATC class is registered in 2 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Catumaxomab is registered in 2 of 19 countries.
Countries holding a registration under ATC L01XC09 (catumaxomab), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 2 of them publish a price we can compare per daily dose
Catumaxomab · ATC L01XC09
2 / 19 countries
- Belgiumprice
- Finlandprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Catumaxomab
- Manufacturer
- Neovii Biotech
- Country
- Belgium (BE)
- ATC code
- L01XC09
- ATC class
- Catumaxomab
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb0754515
- be_apb2883866
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Catumaxomab in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaKORJUNYAtnahs Pharma Netherlands B.V., Amsterdam
- FinlandRemovabNeovii Biotech GmbH
- PolandKORJUNYLindis Biotech GmbH
- SwedenKorjuny 10 mikrogram Koncentrat till infusionsvätska, lösningAtnahs Pharma Netherlands B.V.
- SpainKORJUNY 10 MICROGRAMOS CONCENTRADO PARA SOLUCION PARA PERFUSIONAtnahs Pharma Netherlands Bv.
- IrelandKorjuny 10 micrograms concentrate for solution for infusionAtnahs Pharma Netherlands B.V.
- IcelandKorjunyAtnahs Pharma Netherlands B.V.
- NetherlandsKorjuny 10 microgram concentraat voor oplossing voor infusieAtnahs Pharma Netherlands B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Korjuny
- Liechtenstein · Korjuny
- Norway · Korjuny
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/edfb4d7e-38db-4df7-85d1-f893def4a937 GET /v1/drugs/edfb4d7e-38db-4df7-85d1-f893def4a937?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": "Concentrate for solution for infusion",
"source": "afmps",
"status": "REVOKED",
"name_en": "Removab 10 µg",
"name_fr": "Removab 10 µg",
"name_nl": "Removab 10 µg",
"amp_code": "SAM342185-00",
"strengths": [
"10.0000"
],
"pack_count": 1,
"substances": [
"Catumaxomab"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Catumaxomab",
"authorisation_numbers": [
"EU/1/09/512/001"
]
}See everything about catumaxomab.
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.