Finland· FI-REL-REL43294
Lymphoseek
A technetium (99mtc) tilmanocept product containing tilmanocept, registered in Finland by Navidea Biopharmaceuticals Europe Ltd.. The same ATC class is registered in 3 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Technetium (99mtc) tilmanocept is registered in 3 of 19 countries.
Countries holding a registration under ATC V09IA09 (technetium (99mtc) tilmanocept), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 3 of them publish a price we can compare per daily dose
Technetium (99mtc) tilmanocept · ATC V09IA09
3 / 19 countries
- Belgiumprice
- Finlandprice
- Norwayprice
The record
At a glance
Fimea (Finland)- Active substance
- Tilmanocept
- Manufacturer
- Navidea Biopharmaceuticals Europe Ltd.
- Country
- Finland (FI)
- ATC code
- V09IA09
- ATC class
- Technetium (99mTc) tilmanocept
- Defined daily dose
- 50 mcg, P
- 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
Technetium (99mtc) tilmanocept in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumLymphoseek 50 µgNavidea Biopharmaceuticals Europe
- SpainLYMPHOSEEK 50 MICROGRAMOS EQUIPO DE REACTIVOS PARA PREPARACION RADIOFARMACEUTICANavidea Biopharmaceuticals Europe Limited
- FranceLYMPHOSEEK 50 microgrammes, trousse pour préparation radiopharmaceutiqueNAVIDEA BIOPHARMACEUTICALS EUROPE (IRLANDE)
- United KingdomLymphoseek 50microgram kit for radiopharmaceutical preparationNorgine Pharmaceuticals Ltd
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/ab3b19c9-5445-4c93-b2da-0c75eca6bb85 GET /v1/drugs/ab3b19c9-5445-4c93-b2da-0c75eca6bb85?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": "valmisteyhdistelmä radioaktiivista lääkettä varten",
"route": "Kasvaimen ympärille",
"ddd_unit": null,
"strength": "50 mikrog",
"atc_label": "teknetium(99mTc)tilmanosepti",
"ma_number": null,
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": "EU/1/14/955/001",
"fimea_rel_id": "REL43294",
"authorised_at": "2014-11-19"
}See everything about technetium (99mtc) tilmanocept.
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.