Poland· PL-100454230
Alpicort
A prednisolone product containing prednisolonum + acidum salicylicum, registered in Poland by Delfarma Sp. z o.o.. 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
Prednisolone is registered in 4 of 19 countries.
Countries holding a registration under ATC D07XA02 (prednisolone), 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
Prednisolone · ATC D07XA02
4 / 19 countries
- Czechiaprice
- Finlandprice
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Prednisolonum + Acidum salicylicum
- Manufacturer
- Delfarma Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- D07XA02
- ATC class
- Prednisolone
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05909991457723
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Prednisolone in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaALPICORTDr. August Wolff GmbH & Co. KG Arzneimittel, Bielefeld
- GermanyAlpicortDr. August Wolff Gmbh & Co. Kg Arzneimittel
Authorised across Europe · EMA
The same active substance is authorised in 9 EEA countries. Names it is sold under:
- Bulgaria · Алпикорт
- Czechia · Alpicort
- Germany · Alpicort, Linola Akut
- Estonia · Alpicort
- Croatia · Alpicort
- Hungary · Alpicort
- Lithuania · Alpicort
- Latvia · Alpicort
- Slovakia · Alpicort
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/0b5202e6-4a12-4274-8678-84b53badebe3 GET /v1/drugs/0b5202e6-4a12-4274-8678-84b53badebe3?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": "Płyn na skórę",
"source": "urpl",
"strength": "(2 mg + 4 mg)/ml",
"packaging": "05909991457723 ¦ Rp ¦ 140805\n1 butelka 100 ml",
"substance": "Prednisolonum 2 mg/ml + Acidum salicylicum 4 mg/ml",
"common_name": "Prednisolonum + Acidum salicylicum",
"pl_product_id": "100454230",
"pozwolenie_nr": "222/21",
"auth_procedure": "IR",
"authorisation_validity": "2026-06-30"
}See everything about prednisolone.
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.