Netherlands· NL-1ec02deb899e
LEMTRADA 12 mg concentraat voor oplossing voor infusie
A alemtuzumab product containing alemtuzumab, registered in Netherlands by Sanofi Belgium. The same ATC class is registered in 11 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Alemtuzumab is registered in 11 of 19 countries.
Countries holding a registration under ATC L04AG06 (alemtuzumab), 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
Alemtuzumab · ATC L04AG06
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- ALEMTUZUMAB
- Manufacturer
- Sanofi Belgium
- Country
- Netherlands (NL)
- ATC code
- L04AG06
- ATC class
- Alemtuzumab
- Defined daily dose
- 0.13 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/13/869
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
338 interactions on record for alemtuzumab.
Graded by severity as the source publishes them — 24 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Alemtuzumab · interactions on record
338 records
- 24 severe
- 314 moderate
Most severe, free to view
- CladribineL01BB04severe
- PrednisoloneA07EA01moderate
- HydrocortisoneA07EA02moderate
- PrednisoneA07EA03moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Alemtuzumab in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomLemtrada 12mg/1.2ml concentrate for solution for infusion vialsSanofi
- FinlandLemtradaSanofi Belgium
- CzechiaCAMPATH
- United StatesCampathGenzyme Corporation
- CanadaLEMTRADASANOFI-AVENTIS CANADA INC
- SpainLEMTRADA 12 MG CONCENTRADO PARA SOLUCION PARA PERFUSIONSanofi Belgium
- SwitzerlandLemtrada
- IrelandLEMTRADA 12 mg concentrate for solution for infusionSanofi Belgium
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Lemtrada
- Liechtenstein · Lemtrada
- Norway · Lemtrada
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/41fd6292-ebf0-4d73-acc6-2f4576021514 GET /v1/drugs/41fd6292-ebf0-4d73-acc6-2f4576021514?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/lemtrada-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Alemtuzumab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp113308",
"excipients": [
"DINATRIUMEDETAAT 2-WATER",
"DINATRIUMWATERSTOFFOSFAAT 2-WATER (E 339)",
"KALIUMCHLORIDE (E 508)",
"KALIUMDIWATERSTOFFOSFAAT 0-WATER (E 340)",
"NATRIUMCHLORIDE",
"POLYSORBAAT 80 (E 433)",
"WATER VOOR INJECTIE"
],
"substances": [
"ALEMTUZUMAB"
],
"leaflet_url": null,
"authorised_at": "2013/09/12",
"procedure_number": "EMEA/H/C/003718",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/13/869",
"additional_monitoring": "Y"
}See everything about alemtuzumab.
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.