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Netherlands· NL-e331d7b1f3e5

Rozlytrek 200 mg harde capsules

A entrectinib product containing entrectinib, registered in Netherlands by Roche Registration GmbH. The same ATC class is registered in 14 of our 19 countries.

ATC L01EX14

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedRozlytrek 200 mg harde capsulesATCL01EX14REGISTER NO.NL-e331d7b1f3e5PACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Entrectinib is registered in 14 of 19 countries.

Countries holding a registration under ATC L01EX14 (entrectinib), 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

Entrectinib · ATC L01EX14

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • 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 entrectinib costs, country by country.

Normalised to the WHO defined daily dose (0.6 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

Entrectinib · price per daily dose (0.6 g)

USD · FX 28 Sept 2026

  • CH Switzerland$216.58
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

CBG-MEB (Netherlands)
Active substance
ENTRECTINIB
Manufacturer
Roche Registration GmbH
Country
Netherlands (NL)
ATC code
L01EX14
ATC class
Entrectinib
Defined daily dose
0.6 g, O
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/20/1460

Regulatory notes

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

Interactions

570 interactions on record for entrectinib.

Graded by severity as the source publishes them — 151 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

Entrectinib · interactions on record

570 records

  • 151 severe
  • 405 moderate
  • 14 minor

Most severe, free to view

  • PapaverineA03AD01severe
  • CisaprideA03FA02severe
  • DolasetronA04AA04severe
  • AprepitantA04AD12severe
  • 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

Entrectinib in 13 other countries

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

All entrectinib products

Authorised across Europe · EMA

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

  • Iceland · Rozlytrek
  • Liechtenstein · Rozlytrek
  • Norway · Rozlytrek

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/ca960cb3-3fd0-4086-b921-1933d8891ac3
GET /v1/drugs/ca960cb3-3fd0-4086-b921-1933d8891ac3?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": "Capsule, hard",
  "route": "Oraal gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/rozlytrek-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Entrectinib",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp126928",
  "excipients": [
    "AMMONIA (E 527)",
    "BLAUWE INKT",
    "CELLULOSE, MICROKRISTALLIJN (E 460(i))",
    "CROSPOVIDON (E 1202)",
    "HYPROMELLOSE (E 464)",
    "HYPROMELLOSE 2910 (3 - 15 mPa.s) (E 464)",
    "INDIGOKARMIJN ALUMINIUMLAK (E 132)",
    "LACTOSE 0-WATER",
    "MAGNESIUMSTEARAAT (E 470b)",
    "PROPYLEENGLYCOL (E 1520)",
    "SCHELLAK (E 904)",
    "SILICIUMDIOXIDE (E 551)",
    "TITAANDIOXIDE (E 171)",
    "WIJNSTEENZUUR, (L (+) Vorm) (E 334)",
    "ZONNEGEEL FCF (E 110)"
  ],
  "substances": [
    "ENTRECTINIB"
  ],
  "leaflet_url": null,
  "authorised_at": "2020/07/31",
  "procedure_number": "EMEA/H/C/004936",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/20/1460",
  "additional_monitoring": "Y"
}

See everything about entrectinib.

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.