Netherlands· NL-17e5e5a0e887
REZUROCK 200 mg, filmomhulde tabletten
A belumosudil product containing belumosudilmesilaat, registered in Netherlands by Sanofi Winthrop Industrie. 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
Belumosudil is registered in 12 of 19 countries.
Countries holding a registration under ATC L04AA48 (belumosudil), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 6 of them publish a price we can compare per daily dose
Belumosudil · ATC L04AA48
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Spainprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- BELUMOSUDILMESILAAT
- Manufacturer
- Sanofi Winthrop Industrie
- Country
- Netherlands (NL)
- ATC code
- L04AA48
- ATC class
- Belumosudil
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/26/2015
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Belumosudil in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaREZUROCKSanofi Winthrop Industrie, Gentilly
- SpainREZUROCK 200 MG COMPRIMIDOS RECUBIERTOS CON PELICULASanofi Winthrop Industrie
- BelgiumRezurock 200 mgSanofi Winthrop Industrie
- IrelandREZUROCK 200 mg film-coated tabletsSanofi Winthrop Industrie
- IcelandREZUROCKSanofi Winthrop Industrie
- SwedenREZUROCK 200 mg Filmdragerad tablettSanofi Winthrop Industrie
- FinlandREZUROCKSanofi Winthrop Industrie
- CanadaREZUROCKSANOFI-AVENTIS CANADA INC
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Rezurock
- Liechtenstein · Rezurock
- Norway · Rezurock
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/8a6cff84-d7aa-4229-8438-f5273b3febbc GET /v1/drugs/8a6cff84-d7aa-4229-8438-f5273b3febbc?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": "Filmomhulde tablet",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/rezurock-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Belumosudil",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp134112",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSCARMELLOSE NATRIUM (E 468)",
"HYPROMELLOSE 2910 (3 - 15 mPa.s) (E 464)",
"IJZEROXIDE GEEL (E 172)",
"MACROGOL",
"MAGNESIUMSTEARAAT (E 470b)",
"POLYVINYLALCOHOL (E 1203)",
"SILICIUMDIOXIDE (E 551)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"BELUMOSUDILMESILAAT"
],
"leaflet_url": null,
"authorised_at": "2026/03/24",
"procedure_number": "EMEA/H/C/006421",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/26/2015",
"additional_monitoring": "Y"
}See everything about belumosudil.
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.