Netherlands· NL-74ec1d97928e
Modalim, tabletten 100 mg
A ciprofibrate product containing ciprofibraat, registered in Netherlands by Sanofi B.V.. The same ATC class is registered in 5 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Ciprofibrate is registered in 5 of 19 countries.
Countries holding a registration under ATC C10AB08 (ciprofibrate), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 3 of them publish a price we can compare per daily dose
Ciprofibrate · ATC C10AB08
5 / 19 countries
- Belgiumprice
- Franceprice
- Netherlands
- Polandprice
- United Kingdom
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- CIPROFIBRAAT
- Manufacturer
- Sanofi B.V.
- Country
- Netherlands (NL)
- ATC code
- C10AB08
- ATC class
- Ciprofibrate
- Defined daily dose
- 0.1 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id17863
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ciprofibrate in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomCiprofibrate 100mg tabletsCST Pharma Ltd
- FranceCIPROFIBRATE ARROW 100 mg, géluleARROW GENERIQUES
- BelgiumCiprofibrate Amdipharm 100 mgAmdipharm
- PolandLipanorSanofi Winthrop Industrie
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Bulgaria · Липанор
- France · Ciprofibrate Arrow, Ciprofibrate Biogaran
- United Kingdom (Northern Ireland) · Ciprofibrate Accord-Uk, Ciprofibrate Zentiva
- Poland · Lipanor
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/2aeae9b7-886a-446a-9f30-eb3dbb2d57d7 GET /v1/drugs/2aeae9b7-886a-446a-9f30-eb3dbb2d57d7?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": "Tablet",
"route": "Oraal gebruik",
"soort": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h17863_smpc.pdf",
"strength": null,
"atc_label": "Ciprofibrate",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg17863",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"HYPROMELLOSE (E 464)",
"LACTOSE 1-WATER",
"MAÏSZETMEEL",
"NATRIUMLAURILSULFAAT",
"STEROTEX K (RI)"
],
"substances": [
"CIPROFIBRAAT"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h17863.pdf",
"authorised_at": "1995/03/28",
"procedure_number": null,
"dispensing_status": "Uitsluitend recept",
"registration_number": "17863",
"additional_monitoring": "N"
}See everything about ciprofibrate.
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.