Poland· PL-100430832
Myditin
A pridinol product containing pridinolum, registered in Poland by Sun-Farm Sp. z o.o.. The same ATC class is registered in 5 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Pridinol is registered in 5 of 19 countries.
Countries holding a registration under ATC M03BX03 (pridinol), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 2 of them publish a price we can compare per daily dose
Pridinol · ATC M03BX03
5 / 19 countries
- Germany
- Japan
- Polandprice
- Switzerlandprice
- United Kingdom
The record
At a glance
URPL (Poland)- Active substance
- Pridinolum
- Manufacturer
- Sun-Farm Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- M03BX03
- ATC class
- Pridinol
- Defined daily dose
- 6 mg, O
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05909991431297
- gtin05907464420809
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pridinol in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandMyopridin 3 mg, TablettenDermapharm AG
- SpainMYDITIN 3 MG COMPRIMIDOS EFGMibe Pharma España S.L.U.
- United KingdomMyopridin 3mg tabletsMibe Pharma UK Ltd
- GermanyMyditinTrommsdorff Gmbh & Co. Kg
Authorised across Europe · EMA
The same active substance is authorised in 5 EEA countries. Names it is sold under:
- Austria · Myopridin
- Germany · Myditin, Myopridin
- Spain · Myditin
- United Kingdom (Northern Ireland) · Myopridin
- Italy · Myditin
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/58f6bc6b-d5bf-4d37-9070-01a663044260 GET /v1/drugs/58f6bc6b-d5bf-4d37-9070-01a663044260?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",
"source": "urpl",
"strength": "3 mg",
"packaging": "05909991431297 ¦ Rp ¦ 136536\n20 tabl.\n05907464420809 ¦ Rp ¦ 145775\n50 tabl.",
"substance": "Pridinol mesylate 3 mg",
"common_name": "Pridinolum",
"pl_product_id": "100430832",
"pozwolenie_nr": "25914",
"auth_procedure": "MRP",
"authorisation_validity": "Bezterminowe"
}See everything about pridinol.
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.