Finland· FI-REL-REL1616
Eldisine
A vindesine product containing vindesine sulfate, registered in Finland by STADA Nordic ApS. The same ATC class is registered in 6 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Vindesine is registered in 6 of 19 countries.
Countries holding a registration under ATC L01CA03 (vindesine), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 4 of them publish a price we can compare per daily dose
Vindesine · ATC L01CA03
6 / 19 countries
- Belgiumprice
- Finlandprice
- Franceprice
- Germany
- Switzerlandprice
- United Kingdom
The record
At a glance
Fimea (Finland)- Active substance
- Vindesine sulfate
- Manufacturer
- STADA Nordic ApS
- Country
- Finland (FI)
- ATC code
- L01CA03
- ATC class
- Vindesine
- 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
Vindesine in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumEldisine 5 mgEG
- SpainENISON 5 MG POLVO PARA SOLUCIoN INYECTABLELaboratorio Stada S.L.
- United KingdomEldisine 5mg powder for solution for injection vialsGenus Pharmaceuticals Ltd
- SwitzerlandEldisine
- GermanyEldisineStadapharm Gmbh
- FranceELDISINE 5 mg, poudre pour solution injectableEG LABO - LABORATOIRES EUROGENERICS
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Germany · Eldisine
- Spain · Enison
- France · Eldisine
- Italy · Eldisine
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/33cc98de-29c9-4399-b9bc-bcdfcdf985ce GET /v1/drugs/33cc98de-29c9-4399-b9bc-bcdfcdf985ce?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": "injektiokuiva-aine, liuosta varten",
"route": null,
"ddd_unit": null,
"strength": "5 mg",
"atc_label": "vindesiini",
"ma_number": "8590",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL1616",
"authorised_at": "1983-11-16"
}See everything about vindesine.
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.