Finland· FI-REL-REL1250
Emovat
A clobetasone product containing clobetasone butyrate, registered in Finland by GlaxoSmithKline Oy. The same ATC class is registered in 7 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Clobetasone is registered in 7 of 19 countries.
Countries holding a registration under ATC D07AB01 (clobetasone), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 3 of them publish a price we can compare per daily dose
Clobetasone · ATC D07AB01
7 / 19 countries
- Belgiumprice
- Canada
- Finlandprice
- Ireland
- Japan
- Switzerlandprice
- United Kingdom
The record
At a glance
Fimea (Finland)- Active substance
- Clobetasone butyrate
- Manufacturer
- GlaxoSmithKline Oy
- Country
- Finland (FI)
- ATC code
- D07AB01
- ATC class
- Clobetasone
- 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
Clobetasone in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumEumovate 0.05 %GlaxoSmithKline Pharmaceuticals
- SwedenEmovat 0,05 % KrämGlaxoSmithKline AB
- CanadaSPECTRO ECZEMACARE MEDICATED CREAMHALEON CANADA ULC
- IrelandEumovate Cream 0.05% w/wGlaxoSmithKline (Ireland) Limited
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Clobavate, Eumovate
- Ireland · Eumovate
- Italy · Clobet, Eumovate
- Sweden · Emovat
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/b0196dfa-0364-4708-9249-76cc7230cb3c GET /v1/drugs/b0196dfa-0364-4708-9249-76cc7230cb3c?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": "voide",
"route": "Iholle",
"ddd_unit": null,
"strength": "0.5 mg/g",
"atc_label": "klobetasoni",
"ma_number": "7663",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL1250",
"authorised_at": "1978-12-13"
}See everything about clobetasone.
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.