Iceland· IS-EU/1/20/1424/001-011
Nustendi
A bempedoic acid and ezetimibe product containing bempedoic acid,ezetimibe, registered in Iceland by DAIICHI SANKYO EUROPE GmbH*. The same ATC class is registered in 10 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Bempedoic acid and ezetimibe is registered in 10 of 19 countries.
Countries holding a registration under ATC C10BA10 (bempedoic acid and ezetimibe), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 7 of them publish a price we can compare per daily dose
Bempedoic acid and ezetimibe · ATC C10BA10
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Bempedoic acid,Ezetimibe
- Manufacturer
- DAIICHI SANKYO EUROPE GmbH*
- Country
- Iceland (IS)
- ATC code
- C10BA10
- ATC class
- Bempedoic acid and ezetimibe
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Bempedoic acid and ezetimibe in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaNUSTENDIDaiichi Sankyo Europe GmbH, Mnichov
- United KingdomNustendi 180mg/10mg tabletsPilsco Ltd
- United StatesNexlizetEsperion Therapeutics, Inc.
- SwitzerlandNustendi 180 mg / 10 mg, FilmtablettenDaiichi Sankyo (Schweiz) AG
- SpainNUSTENDI 180 mg/10 mg COMPRIMIDOS RECUBIERTOS CON PELICULADaiichi Sankyo Europe Gmbh
- NetherlandsNustendi 180 mg/10 mg filmomhulde tablettenDAIICHI SANKYO EUROPE GmbH
- PolandNustendiDaiichi Sankyo Europe GmbH
- SwedenNustendi 180 mg/10 mg Filmdragerad tablettDaiichi Sankyo Europe GmbH
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Liechtenstein · Nustendi
- Norway · Nustendi
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 Icelandic Medicines Agency (Iceland). 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/80f81ae3-fa97-4bba-9ea3-dbd0a0987397 GET /v1/drugs/80f81ae3-fa97-4bba-9ea3-dbd0a0987397?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": "Filmuhúðuð tafla",
"source": "lyfjastofnun",
"atc_raw": "C10BA10",
"marketed": false,
"strength": "180 mg/10 mg",
"ma_number": "EU/1/20/1424/001-011",
"substance": "Bempedoic acid,Ezetimibe",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "43917"
}See everything about bempedoic acid and ezetimibe.
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.