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Czechia· CZ-0238673

XOSPATA

A gilteritinib product containing gilteritinib fumarate, registered in Czechia by Astellas Pharma Europe B.V., Leiden. The same ATC class is registered in 13 of our 19 countries.

ATC L01EX13

Checked against SÚKL (Czech Republic) on

Informational only — not a medical device.

SOURCE REGISTER · CZSÚKL (Czech Republic)normalisedXOSPATAATCL01EX13REGISTER NO.CZ-0238673PACKS LISTED0CHECKEDSeptember 28, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about gilteritinib fumarateAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Gilteritinib is registered in 13 of 19 countries.

Countries holding a registration under ATC L01EX13 (gilteritinib), each read from that country’s own register.

  • This record: Czechia, from SÚKL (Czech Republic)
  • 8 of them publish a price we can compare per daily dose
Search gilteritinib products by name

Gilteritinib · ATC L01EX13

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Japan
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

Price per daily dose

What a daily dose of gilteritinib costs, country by country.

Normalised to the WHO defined daily dose (0.12 g), 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
Open the full comparison — free accountDrug prices for market access

Gilteritinib · price per daily dose (0.12 g)

USD · FX 28 Sept 2026

  • CH Switzerland$662.17
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

SÚKL (Czech Republic)
Active substance
GILTERITINIB FUMARATE
Manufacturer
Astellas Pharma Europe B.V., Leiden
Country
Czechia (CZ)
ATC code
L01EX13
ATC class
Gilteritinib
Defined daily dose
0.12 g, O
Reimbursed
Not published by this register
Source register
SÚKL (Czech Republic)
Last checked
September 28, 2026

Packs & prices · 0

No packs listed by the register for this record.

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

529 interactions on record for gilteritinib.

Graded by severity as the source publishes them — 116 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan
Check gilteritinib against other medicinesHow interaction checks work

Gilteritinib · interactions on record

529 records

  • 116 severe
  • 408 moderate
  • 5 minor

Most severe, free to view

  • PapaverineA03AD01severe
  • CisaprideA03FA02severe
  • DolasetronA04AA04severe
  • LonafarnibA16AX20severe
  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Gilteritinib in 13 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All gilteritinib products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Xospata
  • Liechtenstein · Xospata
  • Norway · Xospata

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 SÚKL (Czech Republic). 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/d7427524-0544-4a08-a6d9-0d0287e46076
GET /v1/drugs/d7427524-0544-4a08-a6d9-0d0287e46076?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": "TBL FLM",
  "source": "sukl",
  "strength": "40MG",
  "pack_size": "84",
  "substance": "GILTERITINIB FUMARATE",
  "cz_kod_sukl": "0238673",
  "product_type": "CH",
  "substance_codes": "22",
  "registration_state": "R",
  "registration_number": "EU/1/19/1399/001"
}
API referenceMCP serverPlans

See everything about gilteritinib.

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.

Try it freeOpen in the console