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United States· US:0069-0231_fa9433bd-5ed2-47c3-84cb-f751c1345f81

Lorbrena

A lorlatinib product containing lorlatinib, registered in United States by Pfizer Laboratories Div Pfizer Inc. The same ATC class is registered in 13 of our 19 countries.

ATC L01ED05US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedLorbrenaATCL01ED05REGISTER NO.US:0069-0231_fa9433bd…PACKS LISTED2CHECKEDJune 26, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about lorlatinibAnswers 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: United States, from FDA National Drug Code directory (United States)
  • 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), the median price runs from $0.31 in France to $192.44 in Switzerland — a ×614 gap.

  • 2 markets 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
  • FR France$0.31
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
LORLATINIB
Manufacturer
Pfizer Laboratories Div Pfizer Inc
Country
United States (US)
ATC code
L01ED05
ATC class
Lorlatinib
Defined daily dose
0.1 g, O
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
June 26, 2026

Packs & prices · 2

  • ndc11
    0069023101
    30 TABLET, FILM COATED in 1 BOTTLE (0069-0231-01)
  • ndc11
    0069-0231-01

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 3 EEA countries. Names it is sold under:

  • Iceland · Lorviqua
  • 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 FDA National Drug Code directory (United States). 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/a23b7a95-5a3d-4307-b411-a72940a3cfc9
GET /v1/drugs/a23b7a95-5a3d-4307-b411-a72940a3cfc9?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.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "100",
  "substance": "LORLATINIB",
  "productndc": "0069-0231",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "NDA210868",
  "marketing_category": "NDA"
}
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