Netherlands· NL-7f01160eafde
Giotrif 30 mg, filmomhulde tabletten
A afatinib product containing afatinibdimaleaat, registered in Netherlands by Boehringer Ingelheim International GmbH. The same ATC class is registered in 12 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Afatinib is registered in 12 of 19 countries.
Countries holding a registration under ATC L01EB03 (afatinib), 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
Afatinib · ATC L01EB03
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of afatinib costs, country by country.
Normalised to the WHO defined daily dose (40 mg), 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
Afatinib · price per daily dose (40 mg)
USD · FX 28 Sept 2026
- CH Switzerland$199.66
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- AFATINIBDIMALEAAT
- Manufacturer
- Boehringer Ingelheim International GmbH
- Country
- Netherlands (NL)
- ATC code
- L01EB03
- ATC class
- Afatinib
- Defined daily dose
- 40 mg, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/13/879
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
170 interactions on record for afatinib.
Graded by severity as the source publishes them — 10 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
Afatinib · interactions on record
170 records
- 10 severe
- 158 moderate
- 2 minor
Most severe, free to view
- MipomersenC10AX11severe
- LomitapideC10AX12severe
- PexidartinibL01EX15severe
- Aminolevulinic acidL01XD04severe
- 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
Afatinib in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwedenGIOTRIF 30 mg Filmdragerad tablettBoehringer Ingelheim International GmbH
- SpainGIOTRIF 30 MG COMPRIMIDOS RECUBIERTOS CON PELICULABoehringer Ingelheim International Gmbh
- FranceGIOTRIF 30 mg, comprimé pelliculéBOEHRINGER INGELHEIM INTERNATIONAL
- IrelandGIOTRIF 30 mg film-coated tabletsBoehringer Ingelheim International GmbH
- IcelandGiotrifBoehringer Ingelheim International GmbH*
- NorwayGiotrifBoehringer Ingelheim International GmbH
- PolandGiotrifBoehringer Ingelheim International GmbH
- SwitzerlandGiotrif
Authorised across Europe · EMA
The same active substance is authorised in 8 EEA countries. Names it is sold under:
- Cyprus · Afatinib Afatinib, Afatinib Sapiens
- Greece · Webrix
- Iceland · Giotrif
- Liechtenstein · Giotrif
- Latvia · Afatinib, Afatinib Lotus
- Malta · Afatinib Lotus
- Norway · Giotrif
- Sweden · Afatinib Lotus, Webrix
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/3d73b7a1-41e8-4002-bc74-507868435133 GET /v1/drugs/3d73b7a1-41e8-4002-bc74-507868435133?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/giotrif-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Afatinib",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp112737",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSPOVIDON (E 1202)",
"HYPROMELLOSE 2910 (3 - 15 mPa.s) (E 464)",
"INDIGOKARMIJN ALUMINIUMLAK (E 132)",
"LACTOSE 1-WATER",
"MACROGOL 400",
"MAGNESIUMSTEARAAT (E 470b)",
"POLYSORBAAT 80 (E 433)",
"SILICIUMDIOXIDE (E 551)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"AFATINIBDIMALEAAT"
],
"leaflet_url": null,
"authorised_at": "2013/09/25",
"procedure_number": "EMEA/H/C/002280",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/13/879",
"additional_monitoring": "Y"
}See everything about afatinib.
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.