France· FR:68902879
YESINTEK 45 mg, solution injectable en stylo prérempli
A ustekinumab product containing ustékinumab, registered in France by BIOSIMILAR COLLABORATIONS IRELAND (IRLANDE), on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
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: France, from Base de données publique des médicaments — BDPM (France)
- 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
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
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- USTÉKINUMAB
- Manufacturer
- BIOSIMILAR COLLABORATIONS IRELAND (IRLANDE)
- Country
- France (FR)
- ATC code
- L04AC05
- ATC class
- Ustekinumab
- Defined daily dose
- 0.54 mg, P
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip1334009303335181 seringue(s) préremplie(s) en verre dans stylo prérempli de 0,5 mLEUR 1.09
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.
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.
- NetherlandsFymskina 45 mg oplossing voor injectie in een voorgevulde spuitFormycon AG
- IrelandPyzchiva 45 mg solution for injection in pre-filled penSamsung Bioepis NL B.V.
- United StatesIMULDOSAAccord BioPharma Inc.
- FinlandABSIMKYAccord Healthcare S.L.U.
- BelgiumAbsimky 130 mgAccord Healthcare
- CzechiaFYMSKINAFormycon AG, Martinsried/Planegg
- SwedenFymskina 130 mg Koncentrat till infusionsvätska, lösningFormycon AG
- PolandAbsimkyAccord Healthcare S.L.U.
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 Base de données publique des médicaments — BDPM (France). 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/e6caca1b-7cc9-4d2e-aabe-3ce4a856f221 GET /v1/drugs/e6caca1b-7cc9-4d2e-aabe-3ce4a856f221?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.
{
"cis": "68902879",
"date_amm": "2025-12-11",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/24/1892",
"substance": "USTÉKINUMAB",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "solution injectable",
"voies_administration": "sous-cutanée",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Oui"
}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.