Netherlands· NL-4bf66dcaa9d8
Columvi 2,5 mg concentraat voor oplossing voor infusie
A other monoclonal antibodies and antibody drug conjugates product containing glofitamab, registered in Netherlands by Roche Registration GmbH. The same ATC class is registered in 5 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Glofitamab is registered in 5 of 19 countries.
Countries holding a registration under ATC L01FX (other monoclonal antibodies and antibody drug conjugates), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 4 of them publish a price we can compare per daily dose
Glofitamab · ATC L01FX
5 / 19 countries
- Finlandprice
- Icelandprice
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- GLOFITAMAB
- Manufacturer
- Roche Registration GmbH
- Country
- Netherlands (NL)
- ATC code
- L01FX
- ATC class
- Other monoclonal antibodies and antibody drug conjugates
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/23/1742
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Glofitamab in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceCOLUMVI 2,5 mg, solution à diluer pour perfusionROCHE REGISTRATION (ALLEMAGNE)
- United StatesColumviGenentech, Inc.
- CanadaCOLUMVIHOFFMANN-LA ROCHE LIMITED
- SwitzerlandColumvi 10 mg/10 ml, Konzentrat zur Herstellung einer InfusionslösungRoche Pharma (Schweiz) AG
- CzechiaCOLUMVIRoche Registration GmbH, Grenzach-Wyhlen
- SpainCOLUMVI 10 MG CONCENTRADO PARA SOLUCION PARA PERFUSIONRoche Registration Gmbh
- FinlandColumviRoche Registration GmbH
- BelgiumColumvi 10 mgRoche Registration
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Columvi
- Liechtenstein · Columvi
- Norway · Columvi
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 CBG-MEB (Netherlands). 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/aa1b8143-bfd5-47c8-95ff-0b944a5c71c4 GET /v1/drugs/aa1b8143-bfd5-47c8-95ff-0b944a5c71c4?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": "Concentraat voor oplossing voor infusie",
"route": "Intraveneus gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/columvi-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Other monoclonal antibodies and antibody drug conjugates",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp129852",
"excipients": [
"HISTIDINE, (L-)",
"HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
"METHIONINE, (L-)",
"POLYSORBAAT 20 (E 432)",
"SACCHAROSE",
"WATER VOOR INJECTIE"
],
"substances": [
"GLOFITAMAB"
],
"leaflet_url": null,
"authorised_at": "2023/07/07",
"procedure_number": "EMEA/H/C/005751",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/23/1742",
"additional_monitoring": "Y"
}See everything about glofitamab.
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.