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Netherlands· NL-0dddbe330556

Lojuxta 40 mg harde capsules

A lomitapide product containing lomitapidemesilaat, registered in Netherlands by Chiesi Farmaceutici S.p.A.. The same ATC class is registered in 14 of our 19 countries.

ATC C10AX12

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedLojuxta 40 mg harde capsulesATCC10AX12REGISTER NO.NL-0dddbe330556PACKS LISTED1CHECKEDJune 30, 2026

Where it is registered

Lomitapide is registered in 14 of 19 countries.

Countries holding a registration under ATC C10AX12 (lomitapide), each read from that country’s own register.

  • This record: Netherlands, from CBG-MEB (Netherlands)
  • 9 of them publish a price we can compare per daily dose

Lomitapide · ATC C10AX12

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Italyprice
  • Netherlands
  • Norwayprice
  • Polandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

CBG-MEB (Netherlands)
Active substance
LOMITAPIDEMESILAAT
Manufacturer
Chiesi Farmaceutici S.p.A.
Country
Netherlands (NL)
ATC code
C10AX12
ATC class
Lomitapide
Defined daily dose
40 mg, O
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
June 30, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/13/851

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

299 interactions on record for lomitapide.

Graded by severity as the source publishes them — 206 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan

Lomitapide · interactions on record

299 records

  • 206 severe
  • 86 moderate
  • 7 minor

Most severe, free to view

  • ClotrimazoleA01AB18severe
  • AprepitantA04AD12severe
  • Chenodeoxycholic acidA05AA01severe
  • SulfasalazineA07EC01severe
  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Lomitapide in 14 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All lomitapide products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Lojuxta
  • Liechtenstein · Lojuxta
  • Norway · Lojuxta

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/54010bbc-e79b-441c-b901-c7e9aae1f6cd
GET /v1/drugs/54010bbc-e79b-441c-b901-c7e9aae1f6cd?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/lojuxta-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Lomitapide",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp117436",
  "excipients": [
    "AMMONIA (E 527)",
    "CELLULOSE, MICROKRISTALLIJN (E 460(i))",
    "GELATINE (E 441)",
    "IJZEROXIDE GEEL (E 172)",
    "IJZEROXIDE ZWART (E 172)",
    "LACTOSE 1-WATER",
    "MAGNESIUMSTEARAAT (E 470b)",
    "MAÏSZETMEEL, GEPREGELATINEERD",
    "NATRIUMZETMEELGLYCOLAAT",
    "PROPYLEENGLYCOL (E 1520)",
    "SCHELLAK GLAZE, GEDEELTELIJK VERESTERD",
    "SILICIUMDIOXIDE (E 551)",
    "TITAANDIOXIDE (E 171)",
    "ZWARTE INKT"
  ],
  "substances": [
    "LOMITAPIDEMESILAAT"
  ],
  "leaflet_url": null,
  "authorised_at": "2016/02/18",
  "procedure_number": "EMEA/H/C/002578",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/13/851",
  "additional_monitoring": "Y"
}

See everything about lomitapide.

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.