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Ireland· IE-PA-EU/1/07/422/005-006

Tasigna 150 mg Capsule, hard

A nilotinib product containing nilotinib, registered in Ireland by Novartis Europharm Limited.

ATC L01XE08

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedTasigna 150 mg Capsule, hardATCL01XE08REGISTER NO.IE-PA-EU/1/07/422/005…PACKS LISTED1CHECKEDSeptember 28, 2026

The record

At a glance

HPRA (Ireland)
Active substance
Nilotinib
Manufacturer
Novartis Europharm Limited
Country
Ireland (IE)
ATC code
L01XE08
ATC class
Nilotinib
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/07/422/005-006

Regulatory notes

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

Interactions

801 interactions on record for nilotinib.

Graded by severity as the source publishes them — 303 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

Nilotinib · interactions on record

801 records

  • 303 severe
  • 433 moderate
  • 20 minor

Most severe, free to view

  • PapaverineA03AD01severe
  • CisaprideA03FA02severe
  • OndansetronA04AA01severe
  • GranisetronA04AA02severe

45 more interactions with mechanism and management, from a commercially licensed source.

Sign in to check
  • 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

Nilotinib in 16 other countries

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

All nilotinib products

Authorised across Europe · EMA

The same active substance is authorised in 30 EEA countries. Names it is sold under:

  • Austria · Nilotinib Stada, Nilotinib Teva
  • Belgium · Nilotinb Eg, Nilotinib
  • Bulgaria · Нилотиниб Зентива, Нилотиниб Стада
  • Cyprus · Nilotinib Bioars, Nilotinib Olpha
  • Czechia · Nilotinib, Nilotinib Stada
  • Germany · Nilotinib Al, Nilotinib Al 150 Mg Hartkapseln Al
  • Denmark · Nilotinib "olpha", Nilotinib Stada
  • Estonia · Nilotinib Olpha, Nilotinib Stada
  • Spain · Nilotinib Cipla, Nilotinib Eugia
  • Finland · Nilotinib Stada, Nilotinib Zentiva
  • France · Nilotinib Arrow, Nilotinib Biogaran
  • United Kingdom (Northern Ireland) · Nilotinib Amarox, Nilotinib Teva Uk
  • Greece · Lobynia, Nilotinib Anabiosis
  • Croatia · Nilmat, Nilotinib Devatis
  • Hungary · Krufton, Nilotinib
  • Iceland · Nilotinib, Nilotinib Accord
  • Italy · Nilotinib Cipla, Nilotinib Eg
  • Liechtenstein · Nilotinib Accord, Tasigna
  • Lithuania · Krufton, Nilotinib Olpha
  • Luxembourg · Nilotinib Eg, Nilotinib Eugia
  • Latvia · Krufton, Nilotinib Olpha
  • Malta · Nilotinib Hydrochloride Dihydrate Clonmel, Nilotinib Olpha
  • Netherlands · Nilotinib Cf, Nilotinib Cipla
  • Norway · Nilotinib Accord, Nilotinib Cipla
  • Poland · Nilotinib Stada, Nilotinib Viatris
  • Portugal · Nilotinib Eugia, Nilotinib Generis
  • Romania · Krufton, Nilotinib Cipla
  • Sweden · Nilotinib Cipla, Nilotinib Devatis
  • Slovenia · Nilmat, Nilotinib Stada
  • Slovakia · Krufton, Nilotinib

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 HPRA (Ireland). 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/e795659f-d227-4766-879e-07f27c602b39
GET /v1/drugs/e795659f-d227-4766-879e-07f27c602b39?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": "Capsule, hard",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "L01XE",
    "L01XE08"
  ],
  "strength": null,
  "pa_number": "EU/1/07/422/005-006",
  "substances": [
    "Nilotinib"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": null,
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": "IC0195-062-001"
}

See everything about nilotinib.

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.