Belgium· BE-AMP-SAM112603-00
Eumovate 0.05 %
A clobetasone product containing clobetasone butyrate, registered in Belgium by GlaxoSmithKline Pharmaceuticals. The same ATC class is registered in 7 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) 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: Belgium, from FAMHP / AFMPS (Belgium)
- 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
FAMHP / AFMPS (Belgium)- Active substance
- Clobetasone Butyrate
- Manufacturer
- GlaxoSmithKline Pharmaceuticals
- Country
- Belgium (BE)
- ATC code
- D07AB01
- ATC class
- Clobetasone
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb0040402
- be_apb0706739
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.
- FinlandCloptisonMerck Sharp & Dohme B.V.
- 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 FAMHP / AFMPS (Belgium). 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/147206a2-6bc8-4d43-a78f-ae9283b4d6bc GET /v1/drugs/147206a2-6bc8-4d43-a78f-ae9283b4d6bc?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": "Ointment",
"source": "afmps",
"status": "REVOKED",
"name_en": "Eumovate 0.05 %",
"name_fr": "Eumovate 0.05 %",
"name_nl": "Eumovate 0.05 %",
"amp_code": "SAM112603-00",
"strengths": [
"0.5000",
"0.5000"
],
"pack_count": 1,
"substances": [
"Clobetasone Butyrate"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Clobetasone",
"authorisation_numbers": [
"BE112603"
]
}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.