Finland· FI-REL-REL60090
AKANTIOR
A polihexanide product containing polihexanide, registered in Finland by SIFI S.p.A. Via Ercole Patti, 36. The same ATC class is registered in 9 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Polihexanide is registered in 9 of 19 countries.
Countries holding a registration under ATC S01AX24 (polihexanide), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 5 of them publish a price we can compare per daily dose
Polihexanide · ATC S01AX24
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- United Kingdom
The record
At a glance
Fimea (Finland)- Active substance
- Polihexanide
- Manufacturer
- SIFI S.p.A. Via Ercole Patti, 36
- Country
- Finland (FI)
- ATC code
- S01AX24
- ATC class
- Polihexanide
- Defined daily dose
- 4 Eindosisbeh
- 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
Polihexanide in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaAKANTIORSIFI S.P.A., ACI SANT'ANTONIO (CT)
- BelgiumAkantior 0.8 mg/mlSIFI
- IrelandAKANTIOR 0.8 mg/mL eye drops, solution in single-dose containerSIFI S.p.A.
- IcelandAKANTIORSIFI S.p.A.
- NetherlandsAKANTIOR 0,8 mg/ml oogdruppels, oplossing in verpakking voor eenmalig gebruikSIFI SpA
- SwedenAKANTIOR 0,8 mg/ml Ögondroppar, lösning i endosbehållareSIFI S.p.A.
- United KingdomAkantior 0.08% eye drops 0.3ml unit doseImported (Italy)
- SwitzerlandLavasept, gebrauchsfertige VerdünnungB. Braun Medical AG
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Iceland · Akantior
- Norway · Akantior
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/048abe77-6d32-4934-b58f-2baf9beb1877 GET /v1/drugs/048abe77-6d32-4934-b58f-2baf9beb1877?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": "silmätipat, liuos, kerta-annospakkaus",
"route": "Silmän pinnalle",
"ddd_unit": null,
"strength": "0.8 mg/ml",
"atc_label": "poliheksanidi",
"ma_number": null,
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": "EU/1/24/1840/001-003",
"fimea_rel_id": "REL60090",
"authorised_at": "2024-08-22"
}See everything about polihexanide.
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.