Belgium· BE-AMP-SAM116663-00
Eldisine 5 mg
A vindesine product containing vindesine sulfate, registered in Belgium by EG. The same ATC class is registered in 6 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) 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: Belgium, from FAMHP / AFMPS (Belgium)
- 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
FAMHP / AFMPS (Belgium)- Active substance
- Vindesine Sulfate
- Manufacturer
- EG
- Country
- Belgium (BE)
- ATC code
- L01CA03
- ATC class
- Vindesine
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb0808816
- be_apb0706069
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.
- SpainENISON 5 MG POLVO PARA SOLUCIoN INYECTABLELaboratorio Stada S.L.
- FinlandEldisineSTADA Nordic ApS
- 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 FAMHP / AFMPS (Belgium). 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/26f79dd6-0bbc-48bc-8d25-94046a03a2af GET /v1/drugs/26f79dd6-0bbc-48bc-8d25-94046a03a2af?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.
{
"form": "Powder for solution for injection",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Eldisine 5 mg",
"name_fr": "Eldisine 5 mg",
"name_nl": "Eldisine 5 mg",
"amp_code": "SAM116663-00",
"strengths": [
"5.0000",
"5.0000",
"5.0000",
"25.0000"
],
"pack_count": 1,
"substances": [
"Vindesine Sulfate",
"Mannitol",
"Sodium Hydroxide"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Vindesine",
"authorisation_numbers": [
"BE116663"
]
}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.