Netherlands· NL-c7dd6e8fca8e
Krazati 200 mg, filmomhulde tablet
A adagrasib product containing adagrasib, registered in Netherlands by Bristol-Myers Squibb Pharma EEIG. The same ATC class is registered in 9 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Adagrasib is registered in 9 of 19 countries.
Countries holding a registration under ATC L01XX77 (adagrasib), 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
Adagrasib · ATC L01XX77
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- ADAGRASIB
- Manufacturer
- Bristol-Myers Squibb Pharma EEIG
- Country
- Netherlands (NL)
- ATC code
- L01XX77
- ATC class
- Adagrasib
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/23/1744
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Adagrasib in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaKRAZATIBristol-Myers Squibb Pharma EEIG, Dublin
- FinlandKRAZATIBristol-Myers Squibb Pharma EEIG
- BelgiumKrazati 200 mgBristol-Myers Squibb Pharma
- IcelandKrazatiBristol-Myers Squibb Pharma EEIG
- PolandKrazatiBristol-Myers Squibb Pharma EEIG
- SwedenKRAZATI 200 mg Filmdragerad tablettBristol-Myers Squibb Pharma EEIG
- IrelandKRAZATI 200 mg film-coated tabletsBristol-Myers Squibb Pharma EEIG
- United StatesKRAZATIMirati Therapeutics, Inc
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Krazati
- Liechtenstein · Krazati
- Norway · Krazati
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/808c2a90-bc98-4be4-9be3-42edbc794f7f GET /v1/drugs/808c2a90-bc98-4be4-9be3-42edbc794f7f?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/krazati-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Adagrasib",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp130003",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSPOVIDON (E 1202)",
"HYPROMELLOSE (E 464)",
"MAGNESIUMSTEARAAT (E 470b)",
"MALTODEXTRINE",
"MANNITOL (D-) (E 421)",
"POLYDEXTROSE (E 1200)",
"SILICIUMDIOXIDE (E 551)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)",
"TRIGLYCERIDEN MIDDELLANGE KETEN"
],
"substances": [
"ADAGRASIB"
],
"leaflet_url": null,
"authorised_at": "2024/01/05",
"procedure_number": "EMEA/H/C/006013",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/23/1744",
"additional_monitoring": "Y"
}See everything about adagrasib.
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.