Finland· FI-REL-REL49211
Lutathera
A lutetium (177lu) oxodotreotide product containing lutetium (177lu) oxodotreotide, registered in Finland by Novartis Europharm Limited. The same ATC class is registered in 11 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Lutetium (177lu) oxodotreotide is registered in 11 of 19 countries.
Countries holding a registration under ATC V10XX04 (lutetium (177lu) oxodotreotide), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 7 of them publish a price we can compare per daily dose
Lutetium (177lu) oxodotreotide · ATC V10XX04
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
Fimea (Finland)- Active substance
- Lutetium (177Lu) oxodotreotide
- Manufacturer
- Novartis Europharm Limited
- Country
- Finland (FI)
- ATC code
- V10XX04
- ATC class
- Lutetium (177Lu) oxodotreotide
- Reimbursed
- Not published by this register
- Source register
- Fimea (Finland)
- Last checked
- September 27, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Lutetium (177lu) oxodotreotide in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaLUTATHERANovartis Europharm Limited, Dublin
- United StatesBEXLUTRYCurium US LLC
- CanadaLUTATHERANOVARTIS PHARMACEUTICALS CANADA INC
- NetherlandsLutathera 370 MBq/ml, oplossing voor infusieNovartis Europharm Limited
- NorwayLutatheraNovartis Europharm Limited
- SwedenLutathera 370 MBq/ml Infusionsvätska, lösningNovartis Europharm Limited
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Lutathera
- Liechtenstein · Lutathera
- Norway · Lutathera
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 Fimea (Finland). 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/187a39eb-0220-42d4-a8d6-86dcbcaed80b GET /v1/drugs/187a39eb-0220-42d4-a8d6-86dcbcaed80b?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.
{
"ddd": null,
"form": "infuusioneste, liuos",
"route": "Laskimoon",
"ddd_unit": null,
"strength": "370 MBq/ml",
"atc_label": "lutetium(177Lu)oksodotreotidi",
"ma_number": null,
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": "EU/1/17/1226/001",
"fimea_rel_id": "REL49211",
"authorised_at": "2017-09-26"
}See everything about lutetium (177lu) oxodotreotide.
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.