Germany· DE-A57-f68e84d059d79d49
Eldisine
A vindesine product containing vindesine sulfate, registered in Germany by Stadapharm Gmbh. The same ATC class is registered in 6 of our 19 countries.
Checked against EMA Article 57 (European Union) 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: Germany, from EMA Article 57 (European Union)
- 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
EMA Article 57 (European Union)- Active substance
- Vindesine Sulfate
- Manufacturer
- Stadapharm Gmbh
- Country
- Germany (DE)
- ATC code
- L01CA03
- ATC class
- Vindesine
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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
- SwitzerlandEldisine
- SpainENISON 5 MG POLVO PARA SOLUCIoN INYECTABLELaboratorio Stada S.L.
- FinlandEldisineSTADA Nordic ApS
- FranceELDISINE 5 mg, poudre pour solution injectableEG LABO - LABORATOIRES EUROGENERICS
- United KingdomEldisine 5mg powder for solution for injection vialsGenus Pharmaceuticals Ltd
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- 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 EMA Article 57 (European Union). 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/201411b3-90ff-4aaa-9a94-262b6cc48f45 GET /v1/drugs/201411b3-90ff-4aaa-9a94-262b6cc48f45?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.
{
"pzn": null,
"route": "Intravenous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Vindesine Sulfate",
"atc_from_source": null,
"authorisation_country": "Germany"
}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.