Netherlands· NL-a7451ffc015a

Ordspono 2 mg concentraat voor oplossing voor infusie

A odronextamab product containing odronextamab, registered in Netherlands by Regeneron Ireland Designated Activity Company. The same ATC class is registered in 6 of our 19 countries.

ATC L01FX34

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

Informational only — not a medical device.

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Where it is registered

Odronextamab is registered in 6 of 19 countries.

Countries holding a registration under ATC L01FX34 (odronextamab), each read from that country’s own register.

This record: Netherlands, from CBG-MEB (Netherlands)
3 of them publish a price we can compare per daily dose

Search odronextamab products by name

Odronextamab · ATC L01FX34

6 / 19 countries

Belgiumprice
Czechiaprice
Denmark
Finlandprice
Ireland
Netherlands

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: ODRONEXTAMAB
Manufacturer: Regeneron Ireland Designated Activity Company
Country: Netherlands (NL)
ATC code: L01FX34
ATC class: Odronextamab
Defined daily dose: 12.86 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/1/24/1843

Regulatory notes

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

Same medicine, other countries

Odronextamab in 8 other countries

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

All odronextamab products

Authorised across Europe · EMA

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

Iceland · Ordspono
Liechtenstein · Ordspono
Norway · Ordspono

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/34ab45aa-d329-429c-a4e7-cf3f86df695e
GET /v1/drugs/34ab45aa-d329-429c-a4e7-cf3f86df695e?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/ordspono-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Odronextamab",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp131968",
  "excipients": [
    "HISTIDINE, (L-)",
    "HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
    "POLYSORBAAT 80 (E 433)",
    "SACCHAROSE",
    "WATER VOOR INJECTIE"
  ],
  "substances": [
    "ODRONEXTAMAB"
  ],
  "leaflet_url": null,
  "authorised_at": "2024/08/22",
  "procedure_number": "EMEA/H/C/006215",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/24/1843",
  "additional_monitoring": "Y"
}

API reference MCP server Plans

See everything about odronextamab.

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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