Netherlands· NL-7ac4410e5ab3
AUGTYRO 40 mg harde capsules
A repotrectinib product containing repotrectinib, registered in Netherlands by Bristol-Myers Squibb Pharma EEIG. The same ATC class is registered in 10 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Repotrectinib is registered in 10 of 19 countries.
Countries holding a registration under ATC L01EX28 (repotrectinib), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 6 of them publish a price we can compare per daily dose
Repotrectinib · ATC L01EX28
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- REPOTRECTINIB
- Manufacturer
- Bristol-Myers Squibb Pharma EEIG
- Country
- Netherlands (NL)
- ATC code
- L01EX28
- ATC class
- Repotrectinib
- Defined daily dose
- 0.32 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/24/1883
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Repotrectinib in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaAUGTYRO
- United StatesAugtyroE.R. Squibb & Sons, L.L.C.
- IrelandAUGTYRO 40 mg hard capsulesBristol-Myers Squibb Pharma EEIG
- BelgiumAugtyro 40 mgBristol-Myers Squibb Pharma
- NorwayAugtyroBristol-Myers Squibb Pharma EEIG
- PolandAugtyroBristol-Myers Squibb Pharma EEIG
- SwedenAugtyro 40 mg Kapsel, hårdBristol-Myers Squibb Pharma EEIG
- IcelandAugtyroBristol-Myers Squibb Pharma EEIG
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Augtyro
- Liechtenstein · Augtyro
- Norway · Augtyro
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/f302a7a2-5750-4594-8f32-3b8a89ea5958 GET /v1/drugs/f302a7a2-5750-4594-8f32-3b8a89ea5958?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/augtyro-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Repotrectinib",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp132613",
"excipients": [
"BLAUWE INKT",
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSCARMELLOSE NATRIUM (E 468)",
"GELATINE (E 441)",
"INDIGOKARMIJN ALUMINIUMLAK (E 132)",
"NATRIUMLAURILSULFAAT",
"SCHELLAK (E 904)",
"SILICIUMDIOXIDE (E 551)",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"REPOTRECTINIB"
],
"leaflet_url": null,
"authorised_at": "2025/01/13",
"procedure_number": "EMEA/H/C/006005",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/24/1883",
"additional_monitoring": "Y"
}See everything about repotrectinib.
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.