Finland· FI-REL-REL4501
Isathal Vet.
A fusidiinihappo product containing fusidic acid hemihydrate, registered in Finland by Dechra Veterinary Products A/S. The same ATC class is registered in 2 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Fusidic acid hemihydrate is registered in 2 of 19 countries.
Countries holding a registration under ATC QS01AA13 (fusidiinihappo), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 1 of them publish a price we can compare per daily dose
Fusidic acid hemihydrate · ATC QS01AA13
2 / 19 countries
- Denmark
- Finlandprice
The record
At a glance
Fimea (Finland)- Active substance
- Fusidic acid hemihydrate
- Manufacturer
- Dechra Veterinary Products A/S
- Country
- Finland (FI)
- ATC code
- QS01AA13
- ATC class
- Fusidiinihappo
- 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
Fusidic acid hemihydrate in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumAffusine 20 mg/gWill Pharma
- NorwayFucithalmicAmdipharm
- GermanyFucidineLeo Pharma A/S
- IrelandFucidin 20 mg/g creamLeo Laboratories Limited
- CzechiaFUCITHALMICAMDIPHARM LIMITED, Dublin
- SwedenFucithalmic 1 % ÖgonsalvaAmdipharm Limited
Authorised across Europe · EMA
The same active substance is authorised in 10 EEA countries. Names it is sold under:
- Bulgaria · Фуситалмик
- Germany · Fucithalmic
- Greece · Fusidic Αcid Promopharma
- Ireland · Fucithalmic
- Italy · Fucithalmic
- Malta · Fucithalmic
- Norway · Fucithalmic
- Poland · Fusacid
- Romania · Fucithalmic
- Sweden · Fucithalmic
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/35b0e41c-b0be-4706-9971-622cb77c7767 GET /v1/drugs/35b0e41c-b0be-4706-9971-622cb77c7767?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, suspensio",
"route": "Silmän pinnalle",
"ddd_unit": null,
"strength": "1 %",
"atc_label": "Fusidiinihappo",
"ma_number": "12375",
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": null,
"fimea_rel_id": "REL4501",
"authorised_at": "1997-09-15"
}See everything about fusidic acid hemihydrate.
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.