Poland· PL-100230814

Stelara

A ustekinumab product containing ustekinumabum, registered in Poland by Janssen-Cilag International N.V.. The same ATC class is registered in 14 of our 19 countries.

ATC L04AC05

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedStelaraATCL04AC05REGISTER NO.PL-100230814PACKS LISTED3CHECKEDSeptember 27, 2026

Where it is registered

Ustekinumab is registered in 14 of 19 countries.

Countries holding a registration under ATC L04AC05 (ustekinumab), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 9 of them publish a price we can compare per daily dose

Ustekinumab · ATC L04AC05

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

Price per daily dose

What a daily dose of ustekinumab costs, country by country.

Normalised to the WHO defined daily dose (0.54 mg), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Ustekinumab · price per daily dose (0.54 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$7.71
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

URPL (Poland)
Active substance
Ustekinumabum
Manufacturer
Janssen-Cilag International N.V.
Country
Poland (PL)
ATC code
L04AC05
ATC class
Ustekinumab
Defined daily dose
0.54 mg, P
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 3

  • gtin
    05909997077512
  • gtin
    05413868122589
  • gtin
    04150184954104

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

399 interactions on record for ustekinumab.

Graded by severity as the source publishes them — 30 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan

Ustekinumab · interactions on record

399 records

  • 30 severe
  • 362 moderate
  • 7 minor

Most severe, free to view

  • CladribineL01BB04severe
  • PrednisoloneA07EA01moderate
  • HydrocortisoneA07EA02moderate
  • PrednisoneA07EA03moderate
  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Ustekinumab in 16 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All ustekinumab products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Imuldosa, Uzpruvo
  • Iceland · Fymskina, Imuldosa
  • Liechtenstein · Fymskina, Imuldosa
  • Norway · Fymskina, Imuldosa

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 URPL (Poland). 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/f62d4091-b21b-4a77-bca4-d98f17199e16
GET /v1/drugs/f62d4091-b21b-4a77-bca4-d98f17199e16?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": "Roztwór do wstrzykiwań",
  "source": "urpl",
  "strength": "90 mg",
  "packaging": "05909997077512 ¦ Rpz ¦ EU/1/08/494/004 ¦ 59668\n1 amp.-strzyk. 1 ml\n05413868122589 ¦ Rpz ¦ EU/1/08/494/007 ¦ 151218\n1 wstrzykiwacz 1 ml\n¦ UR/Z/4c/119/23 - 04150184954104",
  "substance": "Ustekinumabum 90 mg",
  "common_name": "Ustekinumabum",
  "pl_product_id": "100230814",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about ustekinumab.

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.