Netherlands· NL-51e4cf2b980c
Xolremdi 100 mg harde capsule
A mavorixafor product containing mavorixafor, registered in Netherlands by Norgine B.V.. The same ATC class is registered in 7 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Mavorixafor is registered in 7 of 19 countries.
Countries holding a registration under ATC L03AX24 (mavorixafor), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 5 of them publish a price we can compare per daily dose
Mavorixafor · ATC L03AX24
7 / 19 countries
- Belgiumprice
- Czechiaprice
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- MAVORIXAFOR
- Manufacturer
- Norgine B.V.
- Country
- Netherlands (NL)
- ATC code
- L03AX24
- ATC class
- Mavorixafor
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/26/2017
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Mavorixafor in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaXOLREMDINorgine B.V., Amsterdam
- FinlandXolremdiNorgine B.V.
- BelgiumXolremdi 100 mgNorgine
- IcelandXolremdiNorgine B.V.
- PolandXolremdiX4 Pharmaceuticals (Austria) GmbH
- SwedenXolremdi 100 mg Kapsel, hårdNorgine BV
- IrelandXolremdi 100mg hard capsuleNorgine B.V.
- United StatesXOLREMDIX4 Pharmaceuticals, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Xolremdi
- Liechtenstein · Xolremdi
- Norway · Xolremdi
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/f7dd7173-19d2-41ad-946a-e6bec145d4ba GET /v1/drugs/f7dd7173-19d2-41ad-946a-e6bec145d4ba?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": "Capsule, hard",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/xolremdi-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Mavorixafor",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp134587",
"excipients": [
"CALCIUMWATERSTOFFOSFAAT 2-WATER (E 341)",
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSCARMELLOSE NATRIUM (E 468)",
"GELATINE (E 441)",
"IJZEROXIDE ZWART (E 172)",
"INDIGOKARMIJN (E 132)",
"NATRIUMLAURILSULFAAT",
"NATRIUMSTEARYLFUMARAAT",
"SCHELLAK GLAZE, GEDEELTELIJK VERESTERD",
"SILICIUMDIOXIDE (E 551)",
"TITAANDIOXIDE (E 171)",
"ZWARTE INKT"
],
"substances": [
"MAVORIXAFOR"
],
"leaflet_url": null,
"authorised_at": "2026/04/27",
"procedure_number": "EMEA/H/C/006496",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/26/2017",
"additional_monitoring": "Y"
}See everything about mavorixafor.
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.