Poland· PL-100525910
Ogsiveo
A other antineoplastic agents product containing nirogacestatum, registered in Poland by SpringWorks Therapeutics Ireland Limited. 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
Nirogacestatum is registered in 5 of 19 countries.
Countries holding a registration under ATC L01XX (other antineoplastic agents), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 3 of them publish a price we can compare per daily dose
Nirogacestatum · ATC L01XX
5 / 19 countries
- Denmark
- Finlandprice
- Ireland
- Polandprice
- United Statesprice
The record
At a glance
URPL (Poland)- Active substance
- Nirogacestatum
- Manufacturer
- SpringWorks Therapeutics Ireland Limited
- Country
- Poland (PL)
- ATC code
- L01XX
- ATC class
- Other antineoplastic agents
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin04150197598227
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Nirogacestatum in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesOGSIVEOSpringWorks Therapeutics, Inc.
- SwitzerlandOgsiveo 150 mg, FilmtablettenMerck (Schweiz) AG
- CzechiaOGSIVEOMerck Europe B.V., Amsterdam
- SpainOGSIVEO 150 MG COMPRIMIDOS RECUBIERTOS CON PELICULAMerck Europe B.V.
- FinlandOgsiveoMerck Europe B.V.
- BelgiumOgsiveo 150 mgMerck Europe
- IrelandOgsiveo 150 mg film‑coated tabletsMerck Europe B.V.
- IcelandOgsiveoMerck Europe B.V.*
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Ogsiveo
- Liechtenstein · Ogsiveo
- Norway · Ogsiveo
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/d6975ff1-755d-4394-b1f2-b7fbbc9452fa GET /v1/drugs/d6975ff1-755d-4394-b1f2-b7fbbc9452fa?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": "150 mg",
"packaging": "Rp ¦ EU/1/25/1932/004 ¦ 163964\n56 tabl.\n¦ UR/Z/4b/102/26 - 04150197598227 ¦ UR/Z/4b/182/26 - 04150197598227 ¦ UR/Z/4b/246/26 - 04150197598227",
"substance": "Nirogacestatum 150 mg",
"common_name": "Nirogacestatum",
"pl_product_id": "100525910",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about nirogacestatum.
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.