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Iceland· IS-EU/1/19/1355/002

Lorviqua

A lorlatinib product containing lorlatinibum inn, registered in Iceland by Pfizer Europe MA EEIG*. The same ATC class is registered in 13 of our 19 countries.

ATC L01ED05

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedLorviquaATCL01ED05REGISTER NO.IS-EU/1/19/1355/002PACKS LISTED1CHECKEDSeptember 29, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about lorlatinibum innAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Lorlatinib is registered in 13 of 19 countries.

Countries holding a registration under ATC L01ED05 (lorlatinib), each read from that country’s own register.

  • This record: Iceland, from Icelandic Medicines Agency (Iceland)
  • 8 of them publish a price we can compare per daily dose
Search lorlatinib products by name

Lorlatinib · ATC L01ED05

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 lorlatinib costs, country by country.

Normalised to the WHO defined daily dose (0.1 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

Lorlatinib · price per daily dose (0.1 g)

USD · FX 28 Sept 2026

  • CH Switzerland$192.44
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

Icelandic Medicines Agency (Iceland)
Active substance
Lorlatinibum INN
Manufacturer
Pfizer Europe MA EEIG*
Country
Iceland (IS)
ATC code
L01ED05
ATC class
Lorlatinib
Defined daily dose
0.1 g, O
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 2026

Packs & prices · 1

1 priced
  • ean
    169944
    30 stk x1 þpakki
    ISK 851308

Regulatory notes

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

Interactions

570 interactions on record for lorlatinib.

Graded by severity as the source publishes them — 119 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 lorlatinib against other medicinesHow interaction checks work

Lorlatinib · interactions on record

570 records

  • 119 severe
  • 439 moderate
  • 12 minor

Most severe, free to view

  • LonafarnibA16AX20severe
  • BerotralstatB06AC06severe
  • VoxelotorB06AX03severe
  • RanolazineC01EB18severe
  • 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

Lorlatinib in 15 other countries

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

All lorlatinib products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Liechtenstein · Lorviqua
  • Norway · Lorviqua

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 Icelandic Medicines Agency (Iceland). 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/09fef1c9-f9a2-4d14-8f58-c9dc8b0e6889
GET /v1/drugs/09fef1c9-f9a2-4d14-8f58-c9dc8b0e6889?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": "Filmuhúðuð tafla",
  "source": "lyfjastofnun",
  "atc_raw": "L01ED05",
  "marketed": true,
  "strength": "100 mg",
  "ma_number": "EU/1/19/1355/002",
  "substance": "Lorlatinibum INN",
  "other_info": "Ávísun lyfsins er bundin við sérfræðinga í lungnalækningum og krabbameinslækningum.",
  "legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
  "ma_issued_serial": "43591"
}
API referenceMCP serverPlans

See everything about lorlatinib.

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