Netherlands· NL-0587c653680b
Quviviq 25 mg, filmomhulde tablet
A daridorexant product containing daridorexanthydrochloride, registered in Netherlands by Idorsia Pharmaceuticals Deutschland GmbH. The same ATC class is registered in 15 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Daridorexant is registered in 15 of 19 countries.
Countries holding a registration under ATC N05CJ03 (daridorexant), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 10 of them publish a price we can compare per daily dose
Daridorexant · ATC N05CJ03
15 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Spainprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of daridorexant costs, country by country.
Normalised to the WHO defined daily dose (50 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
Daridorexant · price per daily dose (50 mg)
USD · FX 28 Sept 2026
- FR France$3.24
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- DARIDOREXANTHYDROCHLORIDE
- Manufacturer
- Idorsia Pharmaceuticals Deutschland GmbH
- Country
- Netherlands (NL)
- ATC code
- N05CJ03
- ATC class
- Daridorexant
- Defined daily dose
- 50 mg, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/22/1638
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Daridorexant in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaQUVIVIQIdorsia Pharmaceuticals Deutschland GmbH, Lörrach
- SwitzerlandQUVIVIQ 25 mg , FilmtablettenIdorsia Pharmaceuticals Ltd
- FinlandQUVIVIQIdorsia Pharmaceuticals Deutschland GmbH
- FranceQUVIVIQ 25 mg, comprimé pelliculéIDORSIA PHARMACEUTICALS DEUTSCHLAND (ALLEMAGNE)
- IrelandQUVIVIQ 25 mg film-coated tabletsIdorsia Pharmaceuticals Deutschland GmbH
- IcelandQuviviqIdorsia Pharmaceuticals Deutschland GmbH
- PolandQUVIVIQIdorsia Pharmaceuticals Deutschland GmbH
- SwedenQUVIVIQ 25 mg Filmdragerad tablettIdorsia Pharmaceuticals Deutschland GmbH
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Quviviq
- Liechtenstein · Quviviq
- Norway · Quviviq
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/d3051c74-9aaa-4d5f-a4fa-d85e0690ea37 GET /v1/drugs/d3051c74-9aaa-4d5f-a4fa-d85e0690ea37?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/quviviq-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Daridorexant",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp128078",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"CROSCARMELLOSE NATRIUM (E 468)",
"GLYCEROL (E 422)",
"HYPROMELLOSE (E 464)",
"IJZEROXIDE ROOD (E 172)",
"IJZEROXIDE ZWART (E 172)",
"MAGNESIUMSTEARAAT (E 470b)",
"MANNITOL (D-) (E 421)",
"POVIDON K 30 (E 1201)",
"SILICIUMDIOXIDE (E 551)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"DARIDOREXANTHYDROCHLORIDE"
],
"leaflet_url": null,
"authorised_at": "2022/04/29",
"procedure_number": "EMEA/H/C/005634",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/22/1638",
"additional_monitoring": "N"
}See everything about daridorexant.
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.