Netherlands· NL-55817b0f60b0

Zelboraf 240 mg, filmomhulde tabletten

A vemurafenib product containing vemurafenib co-precipitaat met hypromelloseacetaatsuccinaat (30-70), registered in Netherlands by Roche Registration GmbH. The same ATC class is registered in 14 of our 19 countries.

ATC L01EC01

Checked against CBG-MEB (Netherlands) on September 29, 2026

Informational only — not a medical device.

Compare price across countriesPer daily dose · free account Ask the assistant about vemurafenib co-precipitaat met hypromelloseacetaatsuccinaat (30-70)Answers with sources · free account Check interactionsSeverity free · mechanism on Growth

Where it is registered

Vemurafenib is registered in 14 of 19 countries.

Countries holding a registration under ATC L01EC01 (vemurafenib), 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

Search vemurafenib products by name

Vemurafenib · ATC L01EC01

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 vemurafenib costs, country by country.

Normalised to the WHO defined daily dose (1.92 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 account Drug prices for market access

Vemurafenib · price per daily dose (1.92 g)

USD · FX 28 Sept 2026

CH Switzerland$263.61

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: VEMURAFENIB CO-PRECIPITAAT MET HYPROMELLOSEACETAATSUCCINAAT (30-70)
Manufacturer: Roche Registration GmbH
Country: Netherlands (NL)
ATC code: L01EC01
ATC class: Vemurafenib
Defined daily dose: 1.92 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/1/12/751

Regulatory notes

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

Interactions

661 interactions on record for vemurafenib.

Graded by severity as the source publishes them — 264 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 vemurafenib against other medicines How interaction checks work

Vemurafenib · interactions on record

661 records

264 severe
377 moderate
20 minor

Most severe, free to view

PapaverineA03AD01severe
CisaprideA03FA02severe
OndansetronA04AA01severe
GranisetronA04AA02severe

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

Vemurafenib in 13 other countries

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

All vemurafenib products

Authorised across Europe · EMA

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

Iceland · Zelboraf
Liechtenstein · Zelboraf
Norway · Zelboraf

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/e803d6c4-0d06-47b5-8998-2eae6538a44f
GET /v1/drugs/e803d6c4-0d06-47b5-8998-2eae6538a44f?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/zelboraf-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Vemurafenib",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp109877",
  "excipients": [
    "CROSCARMELLOSE  NATRIUM  (E 468)",
    "HYPROLOSE (E 463)",
    "IJZEROXIDE ROOD  (E 172)",
    "MACROGOL 3350",
    "MAGNESIUMSTEARAAT (E 470b)",
    "POLYVINYLALCOHOL (E 1203)",
    "SILICIUMDIOXIDE (E 551)",
    "TALK (E 553b)",
    "TITAANDIOXIDE (E 171)"
  ],
  "substances": [
    "VEMURAFENIB CO-PRECIPITAAT MET HYPROMELLOSEACETAATSUCCINAAT (30-70)"
  ],
  "leaflet_url": null,
  "authorised_at": "2012/02/17",
  "procedure_number": "EMEA/H/C/002409",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/12/751",
  "additional_monitoring": "N"
}

API reference MCP server Plans

See everything about vemurafenib.

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.

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