Finland· FI-REL-REL12195
Venofer
A iron, parenteral preparations product containing iron(iii)hydroxide sucrose complex, registered in Finland by Vifor France. 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
Iron(iii)hydroxide sucrose complex is registered in 11 of 19 countries.
Countries holding a registration under ATC B03AC (iron, parenteral preparations), 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
Iron(iii)hydroxide sucrose complex · ATC B03AC
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
Fimea (Finland)- Active substance
- Iron(III)hydroxide sucrose complex
- Manufacturer
- Vifor France
- Country
- Finland (FI)
- ATC code
- B03AC
- ATC class
- Iron, parenteral preparations
- 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 class
Other records under B03AC
Iron, parenteral preparations, as other registers publish it.
- FinlandColleoferVifor France SA
- NorwayCosmoferPharmacosmos
- DenmarkCosmoferPharmacosmos A/S
- FinlandCosmoferPharmacosmos A/S
- PolandCosmoFerPharmacosmos A/S
- NetherlandsCosmoFer 50 mg/ml oplossing voor infusie en injectiePharmacosmos A/S
- IrelandCosmoFer 50 mg/ml solution for infusion and injectionOriginalis B.V.
- NetherlandsCosmoFer 50 mg/ml, oplossing voor infusie en injectieEuro Registratie Collectief B.V.
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/d8cde66e-a65c-4ebb-9c94-ee9b44a32cdb GET /v1/drugs/d8cde66e-a65c-4ebb-9c94-ee9b44a32cdb?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": "0.1",
"form": "injektioneste, liuos/infuusiokonsentraatti, liuosta varten",
"route": "Laskimoon",
"ddd_unit": "g",
"strength": "20 mg/ml",
"atc_label": "Rauta, parenteraaliset valmisteet",
"ma_number": "14727",
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": null,
"fimea_rel_id": "REL12195",
"authorised_at": "2001-01-15"
}See everything about iron(iii)hydroxide sucrose complex.
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.