Netherlands· NL-aa4db4e7175a
Lorviqua, 100 mg filmomhulde tabletten
A lorlatinib product containing lorlatinib, registered in Netherlands by Pfizer Limited. The same ATC class is registered in 13 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
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: Netherlands, from CBG-MEB (Netherlands)
- 8 of them publish a price we can compare per daily dose
Lorlatinib · ATC L01ED05
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
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
Lorlatinib · price per daily dose (0.1 g)
USD · FX 28 Sept 2026
- CH Switzerland$192.44
- FR France$0.31
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- LORLATINIB
- Manufacturer
- Pfizer Limited
- Country
- Netherlands (NL)
- ATC code
- L01ED05
- ATC class
- Lorlatinib
- Defined daily dose
- 0.1 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/19/1355
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
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.
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.
- FinlandLorviquaAbacus Medicine A/S
- NorwayLorviquaPfizer Europe MA EEIG (1)
- United StatesLorbrenaPfizer Laboratories Div Pfizer Inc
- SpainLORVIQUA 100 MG COMPRIMIDOS RECUBIERTOS CON PELÍCULAPfizer Europe Ma Eeig
- FranceLORVIQUA 100 mg, comprimé pelliculéPFIZER EUROPE MA EEIG (BELGIQUE)
- BelgiumLorviqua 100 mgPfizer Europe MA
- IcelandLorviquaPfizer Europe MA EEIG*
- PolandLorviquaPfizer Europe MA EEIG
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 CBG-MEB (Netherlands). 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/b51a7209-8b2c-4ecc-a15c-d866b2100c37 GET /v1/drugs/b51a7209-8b2c-4ecc-a15c-d866b2100c37?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": "Filmomhulde tablet",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/lorviqua-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Lorlatinib",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp122499",
"excipients": [
"CALCIUMWATERSTOFFOSFAAT 0-WATER (E 341)",
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"GLYCEROLTRIACETAAT (E 1518)",
"HYPROMELLOSE 2910 (3 - 15 mPa.s) (E 464)",
"IJZEROXIDE ROOD (E 172)",
"IJZEROXIDE ZWART (E 172)",
"LACTOSE 1-WATER",
"MACROGOL 3350",
"MAGNESIUMSTEARAAT (E 470b)",
"NATRIUMZETMEELGLYCOLAAT",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"LORLATINIB"
],
"leaflet_url": null,
"authorised_at": "2019/05/06",
"procedure_number": "EMEA/H/C/004646",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/19/1355",
"additional_monitoring": "Y"
}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.