Netherlands· NL-132431fe33a1
Lunsumio 45 mg oplossing voor injectie
A mosunetuzumab product containing mosunetuzumab, registered in Netherlands by Roche Registration GmbH. The same ATC class is registered in 12 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Mosunetuzumab is registered in 12 of 19 countries.
Countries holding a registration under ATC L01FX25 (mosunetuzumab), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 7 of them publish a price we can compare per daily dose
Mosunetuzumab · ATC L01FX25
12 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- MOSUNETUZUMAB
- Manufacturer
- Roche Registration GmbH
- Country
- Netherlands (NL)
- ATC code
- L01FX25
- ATC class
- Mosunetuzumab
- Defined daily dose
- 1.8 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/22/1649
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Mosunetuzumab in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- IrelandLunsumio 45 mg solution for injectionRoche Registration GmbH
- United StatesLunsumioGenentech, Inc.
- FinlandLunsumioOrifarm Oy
- CzechiaLUNSUMIORoche Registration GmbH, Grenzach-Wyhlen
- SpainLUNSUMIO 1 MG CONCENTRADO PARA SOLUCION PARA PERFUSIONRoche Registration Gmbh
- BelgiumLunsumio 1 mgRoche Registration
- IcelandLunsumioRoche Registration GmbH*
- Japanモスネツズマブ(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 · Lunsumio
- Liechtenstein · Lunsumio
- Norway · Lunsumio
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/beb6e04f-322f-4479-9bc1-5b2cfba4d163 GET /v1/drugs/beb6e04f-322f-4479-9bc1-5b2cfba4d163?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": "Oplossing voor injectie",
"route": "Subcutaan gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/lunsumio-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Mosunetuzumab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp134405",
"excipients": [
"AZIJNZUUR (E 260), GECONCENTREERD",
"HISTIDINE, (L-)",
"METHIONINE, (L-)",
"POLYSORBAAT 20 (E 432)",
"SACCHAROSE",
"WATER VOOR INJECTIE"
],
"substances": [
"MOSUNETUZUMAB"
],
"leaflet_url": null,
"authorised_at": "2022/06/03",
"procedure_number": "EMEA/H/C/005680",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/22/1649",
"additional_monitoring": "Y"
}See everything about mosunetuzumab.
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.