Netherlands· NL-916809f97cc3
Iqirvo 80 mg filmomhulde tabletten
A elafibranor product containing elafibranor, registered in Netherlands by Ipsen Pharma. 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
Elafibranor is registered in 12 of 19 countries.
Countries holding a registration under ATC A05AX06 (elafibranor), 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
Elafibranor · ATC A05AX06
12 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- ELAFIBRANOR
- Manufacturer
- Ipsen Pharma
- Country
- Netherlands (NL)
- ATC code
- A05AX06
- ATC class
- Elafibranor
- Defined daily dose
- 80 mg, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/24/1855
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Elafibranor in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaIQIRVOIPSEN PHARMA S.A.S., Paříž
- United StatesIQIRVOIpsen Biopharmaceuticals, Inc.
- FinlandIqirvoIpsen Pharma
- FranceIQIRVO 80 mg, comprimé pelliculéIPSEN PHARMA
- BelgiumIqirvo 80 mgIpsen Pharma
- IcelandIqirvoIpsen Pharma
- NorwayIqirvoIpsen Pharma
- PolandIqirvoIpsen Pharma
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Iqirvo
- Liechtenstein · Iqirvo
- Norway · Iqirvo
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/eb118037-e07a-4ae4-b3ae-84a7e3d4df50 GET /v1/drugs/eb118037-e07a-4ae4-b3ae-84a7e3d4df50?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/iqirvo-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Elafibranor",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp132414",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSCARMELLOSE NATRIUM (E 468)",
"IJZEROXIDE GEEL (E 172)",
"IJZEROXIDE ROOD (E 172)",
"MACROGOL",
"MAGNESIUMSTEARAAT (E 470b)",
"POLYVINYLALCOHOL, GEDEELTELIJK GEHYDROLYSEERD (E1203)",
"POVIDON K 30 (E 1201)",
"SILICIUMDIOXIDE (E 551)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"ELAFIBRANOR"
],
"leaflet_url": null,
"authorised_at": "2024/09/19",
"procedure_number": "EMEA/H/C/006231",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/24/1855",
"additional_monitoring": "Y"
}See everything about elafibranor.
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.