Poland· PL-100515267
Lyvdelzi
A other drugs for bile therapy product containing seladelparum, registered in Poland by Gilead Sciences Ireland UC. The same ATC class is registered in 4 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Seladelparum is registered in 4 of 19 countries.
Countries holding a registration under ATC A05AX (other drugs for bile therapy), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 4 of them publish a price we can compare per daily dose
Seladelparum · ATC A05AX
4 / 19 countries
- Belgiumprice
- Czechiaprice
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Seladelparum
- Manufacturer
- Gilead Sciences Ireland UC
- Country
- Poland (PL)
- ATC code
- A05AX
- ATC class
- Other drugs for bile therapy
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 3
- gtin05391507148452
- gtin04150196244477
- gtin04150197439919
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Seladelparum in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandLyvdelzi 10 mg, HartkapselnGilead Sciences Switzerland Sàrl
- SpainLYVDELZI 10 MG CAPSULAS DURASGilead Sciences Ireland Unlimited Company
- United KingdomLivdelzi 10mg capsulesGilead Sciences Ltd
- NetherlandsLyvdelzi 10 mg harde capsulesGilead Sciences Ireland UC
- NorwayLyvdelziGilead Sciences Ireland UC
- SwedenLyvdelzi 10 mg Kapsel, hårdGilead Sciences Ireland UC
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Lyvdelzi
- Liechtenstein · Lyvdelzi
- Norway · Lyvdelzi
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/f16f3699-aadb-4eec-b1b7-1ce2f34f0738 GET /v1/drugs/f16f3699-aadb-4eec-b1b7-1ce2f34f0738?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": "Kapsułki twarde",
"source": "urpl",
"strength": "10 mg",
"packaging": "05391507148452 ¦ Rp ¦ EU/1/24/1898/001 ¦ 161032\n30 kaps. \n¦ UR/Z/4b/110/25 - 04150196244477 ¦ UR/Z/4b/119/25 - 04150196244477 ¦ UR/Z/4b/195/25 - 04150197439919 ¦ UR/Z/4b/293/25 - 04150197439919 ¦ UR/Z/4b/033/26 - 04150197439919",
"substance": "Seladelparum 10 mg",
"common_name": "Seladelparum",
"pl_product_id": "100515267",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about seladelparum.
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.