France· FR:68372441
TREMFYA 100 mg, solution injectable en seringue préremplie
A guselkumab product containing guselkumab, registered in France by JANSSEN CILAG INTERNATIONAL NV, 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
Guselkumab is registered in 14 of 19 countries.
Countries holding a registration under ATC L04AC16 (guselkumab), 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
Guselkumab · ATC L04AC16
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 guselkumab costs, country by country.
Normalised to the WHO defined daily dose (1.79 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
Guselkumab · price per daily dose (1.79 mg)
USD · FX 28 Sept 2026
- CH Switzerland$44.94
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- GUSELKUMAB
- Manufacturer
- JANSSEN CILAG INTERNATIONAL NV
- Country
- France (FR)
- ATC code
- L04AC16
- ATC class
- Guselkumab
- Defined daily dose
- 1.79 mg, P
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip1334009301227541 seringue(s) préremplie(s) en verre de 1 mlEUR 1.8
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
149 interactions on record for guselkumab.
Graded by severity as the source publishes them — 27 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
Guselkumab · interactions on record
149 records
- 27 severe
- 115 moderate
- 7 minor
Most severe, free to view
- CladribineL01BB04severe
- Talimogene laherparepvecL01XL02severe
- Talimogen laherparepvecL01XX51severe
- LeflunomidL04AA13severe
- 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
Guselkumab in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsTremfya 100 mg OnePress oplossing voor injectie in een voorgevulde penJanssen-Cilag International NV
- IrelandTremfya 100 mg Solution for injection pre-filled syringeJanssen-Cilag International NV
- CzechiaTREMFYAJanssen-Cilag International N.V., Beerse
- SwitzerlandTremfya 100 mg/1 ml, Injektionslösung im FertigpenJanssen-Cilag AG
- IcelandTremfyaJanssen-Cilag International NV*
- BelgiumTremfya 100 mgJanssen-Cilag International
- FinlandTremfyaJanssen-Cilag International NV
- SwedenTremfya (OnePress) 100 mg Injektionsvätska, lösning i förfylld injektionspennaJanssen-Cilag International NV
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Tremfya
- Liechtenstein · Tremfya
- Norway · Tremfya
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/be0cdafe-af0f-49bc-9fd2-89682651db34 GET /v1/drugs/be0cdafe-af0f-49bc-9fd2-89682651db34?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": "68372441",
"date_amm": "2017-11-10",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/17/1234",
"substance": "GUSELKUMAB",
"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": "Non"
}See everything about guselkumab.
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.