Sweden· SE-20230727000036
Ordspono 2 mg Koncentrat till infusionsvätska, lösning
A medicinal product containing odronextamab, registered in Sweden by Regeneron Ireland Designated Activity Company.
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Odronextamab
- Manufacturer
- Regeneron Ireland Designated Activity Company
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer20230727000036
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.
- BelgiumOrdspono 2 mgRegeneron Ireland Designated Activity Company (DAC)
- CzechiaORDSPONORegeneron Ireland Designated Activity Company, Dublin
- FinlandOrdsponoRegeneron Ireland Designated Activity Company (DAC)
- IrelandOrdspono 2 mg Concentrate for solution for infusionRegeneron Ireland Designated Activity Company
- IcelandOrdsponoRegeneron Ireland Designated Activity Company
- PolandOrdsponoRegeneron Ireland Designated Activity Company (DAC)
- SpainORDSPONO 2 MG CONCENTRADO PARA SOLUCION PARA PERFUSIONRegeneron Ireland Designated Activity Company
- NetherlandsOrdspono 2 mg concentraat voor oplossing voor infusieRegeneron Ireland Designated Activity Company
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 Swedish Medical Products Agency (Sweden). 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/8a40c8be-e49f-473c-9b74-1773ed903cfa GET /v1/drugs/8a40c8be-e49f-473c-9b74-1773ed903cfa?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.
{
"source": "lakemedelsverket",
"doc_types": [
"EPAR",
"EMA"
],
"se_npl_id": "20230727000036",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20230727000036",
"product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/ordspono-epar-product-information_sv.pdf"
}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.