Netherlands· NL-70e27b193464

LEQEMBI 100 mg/ml concentraat voor oplossing voor infusie

A lecanemab product containing lecanemab, registered in Netherlands by Eisai GmbH. The same ATC class is registered in 10 of our 19 countries.

ATC N06DX04

Checked against CBG-MEB (Netherlands) on September 29, 2026

Informational only — not a medical device.

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Where it is registered

Lecanemab is registered in 10 of 19 countries.

Countries holding a registration under ATC N06DX04 (lecanemab), 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

Search lecanemab products by name

Lecanemab · ATC N06DX04

10 / 19 countries

Belgiumprice
Czechiaprice
Denmark
Finlandprice
Icelandprice
Ireland
Netherlands
Polandprice
United Kingdom
United Statesprice

Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

CBG-MEB (Netherlands)

Active substance: LECANEMAB
Manufacturer: Eisai GmbH
Country: Netherlands (NL)
ATC code: N06DX04
ATC class: Lecanemab
Defined daily dose: 50 mg, P
Reimbursed: Not published by this register
Source register: CBG-MEB (Netherlands)
Last checked: September 29, 2026

Packs & prices · 1

cbg_meb_id
EU/1/24/1891

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Lecanemab in 11 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All lecanemab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

Iceland · Leqembi
Liechtenstein · Leqembi
Norway · Leqembi

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/4e76979e-2a51-4f03-ba6f-f12de02d629c
GET /v1/drugs/4e76979e-2a51-4f03-ba6f-f12de02d629c?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/leqembi-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Lecanemab",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp131054",
  "excipients": [
    "ARGININEHYDROCHLORIDE, (L-)",
    "HISTIDINE, (L-)",
    "HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
    "POLYSORBAAT 80 (E 433)",
    "WATER VOOR INJECTIE"
  ],
  "substances": [
    "LECANEMAB"
  ],
  "leaflet_url": null,
  "authorised_at": "2025/04/15",
  "procedure_number": "EMEA/H/C/005966",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/24/1891",
  "additional_monitoring": "Y"
}

API reference MCP server Plans

See everything about lecanemab.

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.

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