Netherlands· NL-bd1302665e8c
Braftovi 75 mg capsule, hard
A encorafenib product containing encorafenib, registered in Netherlands by Pierre Fabre Medicament. The same ATC class is registered in 14 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Encorafenib is registered in 14 of 19 countries.
Countries holding a registration under ATC L01EC03 (encorafenib), 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
Encorafenib · ATC L01EC03
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of encorafenib costs, country by country.
Normalised to the WHO defined daily dose (0.45 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
Encorafenib · price per daily dose (0.45 g)
USD · FX 28 Sept 2026
- CH Switzerland$238.24
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- ENCORAFENIB
- Manufacturer
- Pierre Fabre Medicament
- Country
- Netherlands (NL)
- ATC code
- L01EC03
- ATC class
- Encorafenib
- Defined daily dose
- 0.45 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/18/1314
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
554 interactions on record for encorafenib.
Graded by severity as the source publishes them — 174 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
Encorafenib · interactions on record
554 records
- 174 severe
- 377 moderate
- 3 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.
Same medicine, other countries
Encorafenib in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaBRAFTOVIPIERRE FABRE MEDICAMENT, Lavaur
- SwitzerlandBraftovi
- United KingdomBraftovi 75mg capsulesPierre Fabre Ltd
- FinlandBraftoviPierre Fabre Medicament
- FranceBRAFTOVI 75 mg, gélulePIERRE FABRE MEDICAMENT
- IrelandBraftovi 75 mg Hard capsulePierre Fabre Medicament
- IcelandBraftoviPierre Fabre Medicament
- NorwayBraftoviPierre Fabre Medicament
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Braftovi
- Liechtenstein · Braftovi
- Norway · Braftovi
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/366fa606-078c-4a5e-bab6-d5d0b99c6245 GET /v1/drugs/366fa606-078c-4a5e-bab6-d5d0b99c6245?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/braftovi-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Encorafenib",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp121738",
"excipients": [
"AMMONIA (E 527)",
"BARNSTEENZUUR (E 363)",
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"COPOVIDON (E 1208)",
"CROSPOVIDON (E 1202)",
"GELATINE (E 441)",
"IJZEROXIDE GEEL (E 172)",
"IJZEROXIDE ROOD (E 172)",
"IJZEROXIDE ZWART (E 172)",
"IJZEROXIDE ZWART (E 172)",
"MAGNESIUMSTEARAAT (E 470b)",
"POLOXAMEER 188",
"PROPYLEENGLYCOL (E 1520)",
"SCHELLAK GLAZE, GEDEELTELIJK VERESTERD",
"SILICIUMDIOXIDE (E 551)",
"TITAANDIOXIDE (E 171)",
"ZWARTE INKT"
],
"substances": [
"ENCORAFENIB"
],
"leaflet_url": null,
"authorised_at": "2018/09/20",
"procedure_number": "EMEA/H/C/004580",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/18/1314",
"additional_monitoring": "N"
}See everything about encorafenib.
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.