Netherlands· NL-f473e75e0b62
AKANTIOR 0,8 mg/ml oogdruppels, oplossing in verpakking voor eenmalig gebruik
A polihexanide product containing polihexanide, registered in Netherlands by SIFI SpA. The same ATC class is registered in 9 of our 19 countries.
Checked against CBG-MEB (Netherlands) 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: Netherlands, from CBG-MEB (Netherlands)
- 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
CBG-MEB (Netherlands)- Active substance
- POLIHEXANIDE
- Manufacturer
- SIFI SpA
- Country
- Netherlands (NL)
- ATC code
- S01AX24
- ATC class
- Polihexanide
- Defined daily dose
- 4 Eindosisbeh
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/24/1840
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
- FinlandAKANTIORSIFI S.p.A. Via Ercole Patti, 36
- IrelandAKANTIOR 0.8 mg/mL eye drops, solution in single-dose containerSIFI S.p.A.
- IcelandAKANTIORSIFI S.p.A.
- 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 CBG-MEB (Netherlands). 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/0c754f1a-ede1-4f22-80e0-17e0ad4ddbd0 GET /v1/drugs/0c754f1a-ede1-4f22-80e0-17e0ad4ddbd0?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": "Oogdruppels, oplossing",
"route": "Oculair gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/akantior-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Polihexanide",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp130018",
"excipients": [
"DINATRIUMWATERSTOFFOSFAAT 12-WATER (E 339)",
"NATRIUMCHLORIDE",
"NATRIUMDIWATERSTOFFOSFAAT 1-WATER (E 339)",
"WATER, GEZUIVERD"
],
"substances": [
"POLIHEXANIDE"
],
"leaflet_url": null,
"authorised_at": "2024/08/22",
"procedure_number": "EMEA/H/C/005858",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/24/1840",
"additional_monitoring": "N"
}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.