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Iceland· IS-EU/1/12/751/001

Zelboraf

A vemurafenib product containing vemurafenibum inn, registered in Iceland by Roche Registration GmbH*. The same ATC class is registered in 14 of our 19 countries.

ATC L01EC01

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedZelborafATCL01EC01REGISTER NO.IS-EU/1/12/751/001PACKS LISTED1CHECKEDSeptember 29, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about vemurafenibum innAnswers with sources · free accountCheck 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: Iceland, from Icelandic Medicines Agency (Iceland)
  • 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 accountDrug 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

Icelandic Medicines Agency (Iceland)
Active substance
Vemurafenibum INN
Manufacturer
Roche Registration GmbH*
Country
Iceland (IS)
ATC code
L01EC01
ATC class
Vemurafenib
Defined daily dose
1.92 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
    438759
    56 stk x1 þpakki
    ISK 278827

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 medicinesHow 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 2 EEA countries. Names it is sold under:

  • 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 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/9f46f964-2e4a-4d4e-91e0-bc0f1f3be047
GET /v1/drugs/9f46f964-2e4a-4d4e-91e0-bc0f1f3be047?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": "L01EC01",
  "marketed": false,
  "strength": "240 mg",
  "ma_number": "EU/1/12/751/001",
  "substance": "Vemurafenibum INN",
  "other_info": "Ávísun lyfsins er bundin við sérfræðinga í krabbameinslækningum.",
  "legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
  "ma_issued_serial": "40956"
}
API referenceMCP serverPlans

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.

Try it freeOpen in the console