Poland· PL-100482203
Sotyktu
A deucravacitinib product containing deucravacitinibum, registered in Poland by Bristol-Myers Squibb Pharma EEIG. The same ATC class is registered in 12 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Deucravacitinib is registered in 12 of 19 countries.
Countries holding a registration under ATC L04AF07 (deucravacitinib), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 7 of them publish a price we can compare per daily dose
Deucravacitinib · ATC L04AF07
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of deucravacitinib costs, country by country.
Normalised to the WHO defined daily dose (6 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
Deucravacitinib · price per daily dose (6 mg)
USD · FX 28 Sept 2026
- FR France$22.97
The record
At a glance
URPL (Poland)- Active substance
- Deucravacitinibum
- Manufacturer
- Bristol-Myers Squibb Pharma EEIG
- Country
- Poland (PL)
- ATC code
- L04AF07
- ATC class
- Deucravacitinib
- Defined daily dose
- 6 mg, O
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin08027950800810
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Deucravacitinib in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaSOTYKTUBristol-Myers Squibb Pharma EEIG, Dublin
- United StatesSOTYKTUE.R. Squibb & Sons, L.L.C.
- FinlandSOTYKTUBristol-Myers Squibb Pharma EEIG
- FranceSOTYKTU 6 mg, comprimé pelliculéBRISTOL-MYERS SQUIBB PHARMA (IRLANDE)
- BelgiumSotyktu 6 mgBristol-Myers Squibb Pharma
- IcelandSOTYKTUBristol-Myers Squibb Pharma EEIG*
- NetherlandsSOTYKTU 6 mg filmomhulde tablettenBristol-Myers Squibb Pharma EEIG
- NorwaySotyktuBristol-Myers Squibb Pharma EEIG
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Sotyktu
- Liechtenstein · Sotyktu
- Norway · Sotyktu
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/2c530e99-bf22-4158-9c87-e676a9b30bb5 GET /v1/drugs/2c530e99-bf22-4158-9c87-e676a9b30bb5?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": "Tabletki powlekane",
"source": "urpl",
"strength": "6 mg",
"packaging": "Rpz ¦ EU/1/23/1718/004 ¦ 149834\n14 tabl. (w blistrze z kalendarzem)\nRpz ¦ EU/1/23/1718/007 ¦ 149835\n84 tabl. (w blistrze bez kalendarza)\nRpz ¦ EU/1/23/1718/003 ¦ 149836\n14 tabl. (w blistrze bez kalendarza)\nRpz ¦ EU/1/23/1718/002 ¦ 149837\n7 tabl. (w blistrze z kalendarzem)\nRpz ¦ EU/1/23/1718/005 ¦ 149838\n28 tabl. (w blistrze bez kalendarza)\nRpz ¦ EU/1/23/1718/008 ¦ 149839\n84 tabl. (w blistrze z kalendarzem)\nRpz ¦ EU/1/23/1718/001 ¦ 149840\n7 tabl. (w blistrze bez kalendarza)\n08027950800810 ¦ Rpz ¦ EU/1/23/1718/006 ¦ 149841\n28 tabl. (w blistrze z kalendarzem)",
"substance": "Deucravacitinibum 6 mg",
"common_name": "Deucravacitinibum",
"pl_product_id": "100482203",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about deucravacitinib.
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.