Ireland· IE-PA-EU/1/22/1650/001-002
Tabrecta 150 mg film-coated tablets
A capmatinib product containing capmatinib dihydrochloride monohydrate, registered in Ireland by Novartis Europharm Limited. The same ATC class is registered in 4 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Capmatinib is registered in 4 of 19 countries.
Countries holding a registration under ATC L01EX17 (capmatinib), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 2 of them publish a price we can compare per daily dose
Capmatinib · ATC L01EX17
4 / 19 countries
- Canada
- Ireland
- Polandprice
- Switzerlandprice
The record
At a glance
HPRA (Ireland)- Active substance
- Capmatinib dihydrochloride monohydrate
- Manufacturer
- Novartis Europharm Limited
- Country
- Ireland (IE)
- ATC code
- L01EX17
- ATC class
- Capmatinib
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/22/1650/001-002
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
173 interactions on record for capmatinib.
Graded by severity as the source publishes them — 28 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
Capmatinib · interactions on record
173 records
- 28 severe
- 136 moderate
- 9 minor
Most severe, free to view
- EdoxabanB01AF03severe
- DexamethasoneH02AB02severe
- KetoconazoleH02CA03severe
- ClarithromycinJ01FA09severe
- 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.
Same medicine, other countries
Capmatinib in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaTABRECTANovartis Europharm Limited, Dublin
- FinlandTabrectaOrifarm Oy
- SpainTABRECTA 150 MG COMPRIMIDOS RECUBIERTOS CON PELICULANovartis Europharm Limited
- IcelandTabrectaNovartis Europharm Limited*
- NetherlandsTabrecta 150mg, filmomhulde tablettenNovartis Europharm Limited
- NorwayTabrectaNovartis Europharm Limited
- PolandTabrectaNovartis Europharm Limited
- SwedenTabrecta 150 mg Filmdragerad tablettNovartis Europharm Limited
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Tabrecta
- Liechtenstein · Tabrecta
- Norway · Tabrecta
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/54126179-fa51-4406-b835-e60b1192005d GET /v1/drugs/54126179-fa51-4406-b835-e60b1192005d?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": "Film-coated tablet",
"routes": [
"Oral use"
],
"source": "hpra",
"atc_all": [
"L01",
"L01EX17"
],
"strength": null,
"pa_number": "EU/1/22/1650/001-002",
"substances": [
"Capmatinib dihydrochloride monohydrate"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "20/06/2022",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about capmatinib.
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.