Poland· PL-100521847

Alyftrek

A other respiratory system products product containing deutivacaftor + tezacaftorum + vanzacaftor, registered in Poland by Vertex Pharmaceuticals (Ireland) Limited. The same ATC class is registered in 6 of our 19 countries.

ATC R07AX

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedAlyftrekATCR07AXREGISTER NO.PL-100521847PACKS LISTED3CHECKEDSeptember 27, 2026

Where it is registered

Deutivacaftor + tezacaftorum + vanzacaftor is registered in 6 of 19 countries.

Countries holding a registration under ATC R07AX (other respiratory system products), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 4 of them publish a price we can compare per daily dose

Deutivacaftor + tezacaftorum + vanzacaftor · ATC R07AX

6 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Ireland
  • Netherlands
  • Polandprice
  • Switzerlandprice
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

URPL (Poland)
Active substance
Deutivacaftor + Tezacaftorum + Vanzacaftor
Manufacturer
Vertex Pharmaceuticals (Ireland) Limited
Country
Poland (PL)
ATC code
R07AX
ATC class
Other respiratory system products
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 3

  • gtin
    00351167179000
  • gtin
    00351167171806
  • gtin
    00351167180808

Regulatory notes

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

Same medicine, other countries

Deutivacaftor + tezacaftorum + vanzacaftor in 10 other countries

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

All deutivacaftor + tezacaftorum + vanzacaftor products

Authorised across Europe · EMA

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

  • Iceland · Alyftrek
  • Liechtenstein · Alyftrek
  • Norway · Alyftrek

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/f3e429ea-93dc-4937-829e-51606ba65588
GET /v1/drugs/f3e429ea-93dc-4937-829e-51606ba65588?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": "50 mg + 20 mg + 4 mg",
  "packaging": "00351167179000 ¦ Rpz ¦ EU/1/25/1943/001 ¦ 162923\n84 tabl.\n¦ UR/Z/4b/206/25 - 00351167171806 ¦ UR/Z/4b/207/25 - 00351167180808",
  "substance": "Deutivacaftor 50 mg + Tezacaftorum 20 mg + Vanzacaftor 4 mg",
  "common_name": "Deutivacaftor + Tezacaftorum + Vanzacaftor",
  "pl_product_id": "100521847",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about deutivacaftor + tezacaftorum + vanzacaftor.

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.