Belgium· BE-AMP-SAM663351-00
Anzupgo 20 mg/g
A delgocitinib product containing delgocitinib, registered in Belgium by Leo Pharma. The same ATC class is registered in 15 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Delgocitinib is registered in 15 of 19 countries.
Countries holding a registration under ATC D11AH11 (delgocitinib), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 10 of them publish a price we can compare per daily dose
Delgocitinib · ATC D11AH11
15 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Delgocitinib
- Manufacturer
- Leo Pharma
- Country
- Belgium (BE)
- ATC code
- D11AH11
- ATC class
- Delgocitinib
- Defined daily dose
- 40 mg, T
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 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
Delgocitinib in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaANZUPGOLEO Pharma A/S, Ballerup
- NorwayAnzupgoLEO
- United StatesAnzupgoLEO Pharma, Inc
- FranceANZUPGO 20 mg/g, crèmeLEO PHARMA A/S (DANEMARK)
- United KingdomAnzupgo 20mg/g creamLEO Pharma
- IrelandAnzupgo 20 mg/g creamLEO Pharma A/S
- SwitzerlandAnzupgo
- ItalyANZUPGO*crema derm 60 g 20 mg/gLEO PHARMA A/S
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Anzupgo
- Iceland · Anzupgo
- Liechtenstein · Anzupgo
- Norway · Anzupgo
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/fcec5df0-ff5e-4bca-b6e8-bc4c6bc9f26a GET /v1/drugs/fcec5df0-ff5e-4bca-b6e8-bc4c6bc9f26a?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": "Cream",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Anzupgo 20 mg/g",
"name_fr": "Anzupgo 20 mg/g",
"name_nl": "Anzupgo 20 mg/g",
"amp_code": "SAM663351-00",
"strengths": [
"20.0000",
"20.0000",
"20.0000",
"10.0000",
"10.0000",
"0.2000",
"0.2000",
"72.0000",
"72.0000"
],
"pack_count": 3,
"substances": [
"Delgocitinib",
"Benzyl Alcohol",
"Butylhydroxyanisole",
"Cetostearyl Alcohol",
"Disodium Edetate"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Delgocitinib",
"authorisation_numbers": [
"EU/1/24/1851/002",
"EU/1/24/1851/001",
"EU/1/24/1851/003"
]
}See everything about delgocitinib.
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.