Netherlands· NL-71eabd9e5ea8
TAKHZYRO 150 mg oplossing voor injectie in voorgevulde spuit
A lanadelumab product containing lanadelumab, registered in Netherlands by Takeda Pharmaceuticals International AG Ireland Branch. The same ATC class is registered in 15 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Lanadelumab is registered in 15 of 19 countries.
Countries holding a registration under ATC B06AC05 (lanadelumab), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 10 of them publish a price we can compare per daily dose
Lanadelumab · ATC B06AC05
15 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of lanadelumab costs, country by country.
Normalised to the WHO defined daily dose (21.4 mg), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Lanadelumab · price per daily dose (21.4 mg)
USD · FX 28 Sept 2026
- CH Switzerland$857.11
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- LANADELUMAB
- Manufacturer
- Takeda Pharmaceuticals International AG Ireland Branch
- Country
- Netherlands (NL)
- ATC code
- B06AC05
- ATC class
- Lanadelumab
- Defined daily dose
- 21.4 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/18/1340
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Lanadelumab in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceTAKHZYRO 150 mg, solution injectable en seringue préremplieTAKEDA PHARMACEUTICALS INTERNATIONAL (IRLANDE)
- IrelandTAKHZYRO 150 mg solution for injection in pre-filled syringeTakeda Pharmaceuticals International AG Ireland Branch
- CzechiaTAKHZYROTakeda Pharmaceuticals International AG Ireland Branch, Dublin
- United StatesTAKHZYROTakeda Pharmaceuticals America, Inc.
- FinlandTakhzyroOrifarm Oy
- BelgiumTakhzyro 150 mgTakeda Pharmaceuticals International Ireland Branch
- United KingdomTakhzyro 150mg/1ml solution for injection pre-filled syringesTakeda UK Ltd
- IcelandTakhzyroTakeda Pharmaceuticals International AG Ireland Branch
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Takhzyro
- Liechtenstein · Takhzyro
- Norway · Takhzyro
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/6593f75f-5a55-4151-9fc0-c4e14f798621 GET /v1/drugs/6593f75f-5a55-4151-9fc0-c4e14f798621?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/takhzyro-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Lanadelumab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp130772",
"excipients": [
"CITROENZUUR 1-WATER (E 330)",
"DINATRIUMWATERSTOFFOSFAAT 2-WATER (E 339)",
"HISTIDINE, (L-)",
"NATRIUMCHLORIDE",
"POLYSORBAAT 80 (E 433)",
"WATER VOOR INJECTIE"
],
"substances": [
"LANADELUMAB"
],
"leaflet_url": null,
"authorised_at": "2018/11/22",
"procedure_number": "EMEA/H/C/004806",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/18/1340",
"additional_monitoring": "N"
}See everything about lanadelumab.
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.