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Czechia· CZ-0272025

VANFLYTA

A quizartinib product containing quizartinib dihydrochloride, registered in Czechia by Daiichi Sankyo Europe GmbH, Mnichov. The same ATC class is registered in 13 of our 19 countries.

ATC L01EX11

Checked against SÚKL (Czech Republic) on

Informational only — not a medical device.

SOURCE REGISTER · CZSÚKL (Czech Republic)normalisedVANFLYTAATCL01EX11REGISTER NO.CZ-0272025PACKS LISTED0CHECKEDSeptember 28, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about quizartinib dihydrochlorideAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Quizartinib is registered in 13 of 19 countries.

Countries holding a registration under ATC L01EX11 (quizartinib), 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 quizartinib products by name

Quizartinib · ATC L01EX11

13 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • 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.

The record

At a glance

SÚKL (Czech Republic)
Active substance
QUIZARTINIB DIHYDROCHLORIDE
Manufacturer
Daiichi Sankyo Europe GmbH, Mnichov
Country
Czechia (CZ)
ATC code
L01EX11
ATC class
Quizartinib
Defined daily dose
53 mg, 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.

Same medicine, other countries

Quizartinib in 13 other countries

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

All quizartinib products

Authorised across Europe · EMA

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

  • Iceland · Vanflyta
  • Liechtenstein · Vanflyta
  • Norway · Vanflyta

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/4c3aa4c0-e53b-44d5-8023-5399a434aa1a
GET /v1/drugs/4c3aa4c0-e53b-44d5-8023-5399a434aa1a?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": "26,5MG",
  "pack_size": "14X1",
  "substance": "QUIZARTINIB DIHYDROCHLORIDE",
  "cz_kod_sukl": "0272025",
  "product_type": "CH",
  "substance_codes": "3362",
  "registration_state": "R",
  "registration_number": "EU/1/23/1768/003"
}
API referenceMCP serverPlans

See everything about quizartinib.

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