Ireland· IE-PA-EU/1/24/1851/001-002
Anzupgo 20 mg/g cream
A delgocitinib product containing delgocitinib, registered in Ireland by LEO Pharma A/S. The same ATC class is registered in 15 of our 19 countries.
Checked against HPRA (Ireland) 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: Ireland, from HPRA (Ireland)
- 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
HPRA (Ireland)- Active substance
- Delgocitinib
- Manufacturer
- LEO Pharma A/S
- Country
- Ireland (IE)
- ATC code
- D11AH11
- ATC class
- Delgocitinib
- Defined daily dose
- 40 mg, T
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/24/1851/001-002
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 PHARMA A/S (Danmark)
- United StatesAnzupgoLEO Pharma, Inc
- FranceANZUPGO 20 mg/g, crèmeLEO PHARMA A/S (DANEMARK)
- SwitzerlandAnzupgo
- NetherlandsAnzupgo 20 mg/g crèmeLeo Pharma A/S
- PolandAnzupgoLEO Pharma A/S
- SwedenAnzupgo 20 mg/g KrämLEO 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 HPRA (Ireland). 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/06a650da-bbad-4bae-b0c9-1745fdebea6b GET /v1/drugs/06a650da-bbad-4bae-b0c9-1745fdebea6b?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",
"routes": [
"Cutaneous use"
],
"source": "hpra",
"atc_all": [
"D11AH11"
],
"strength": null,
"pa_number": "EU/1/24/1851/001-002",
"substances": [
"Delgocitinib"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "19/09/2024",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}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.