Netherlands· NL-a75f328bf0a9
Fintepla 2,2 mg/ml drank
A fenfluramine product containing fenfluramine hydrochloride, registered in Netherlands by UCB Pharma S.A.. The same ATC class is registered in 11 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Fenfluramine is registered in 11 of 19 countries.
Countries holding a registration under ATC N03AX26 (fenfluramine), 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
Fenfluramine · ATC N03AX26
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- FENFLURAMINE HYDROCHLORIDE
- Manufacturer
- UCB Pharma S.A.
- Country
- Netherlands (NL)
- ATC code
- N03AX26
- ATC class
- Fenfluramine
- Defined daily dose
- 8 mg, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/20/1491
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
349 interactions on record for fenfluramine.
Graded by severity as the source publishes them — 85 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
Fenfluramine · interactions on record
349 records
- 85 severe
- 260 moderate
- 4 minor
Most severe, free to view
- OndansetronA04AA01severe
- GranisetronA04AA02severe
- DolasetronA04AA04severe
- PalonosetronA04AA05severe
- 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.
Same medicine, other countries
Fenfluramine in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaFINTEPLAUCB Pharma SA, Brusel
- SwitzerlandFintepla 2.2 mg/ml, solution buvableUCB-Pharma SA
- NorwayFinteplaUCB Nordic AS
- FranceFINTEPLA 2,2 mg/mL, solution buvableUCB PHARMA BELGIQUE
- IrelandFintepla 2.2 mg/ml oral solutionUCB Pharma S.A.
- IcelandFinteplaUCB Pharma S.A.*
- PolandFinteplaUCB Pharma S.A.
- SwedenFintepla 2,2 mg/ml Oral lösningUCB Pharma S.A.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Fintepla
- Liechtenstein · Fintepla
- Norway · Fintepla
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/82289c1f-cdb9-40b6-86b5-1e50fb0fc15b GET /v1/drugs/82289c1f-cdb9-40b6-86b5-1e50fb0fc15b?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": "Drank",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/fintepla-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Fenfluramine",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp124535",
"excipients": [
"ARABISCHE GOM (E 414)",
"CITROENZUUR 1-WATER (E 330)",
"GLUCOSE (HYDRATATIEVORM ONBEKEND)",
"HYDROXYETHYLCELLULOSE",
"KERSENSMAAKSTOF",
"MALTODEXTRINE",
"NATRIUMETHYLPARAHYDROXYBENZOAAT (E 215)",
"NATRIUMMETHYLPARAHYDROXYBENZOAAT (E 219)",
"SUCRALOSE (E 955)",
"TRIKALIUMCITRAAT 1-WATER (E 332)",
"WATER VOOR INJECTIE",
"ZWAVELDIOXIDE (E 220)"
],
"substances": [
"FENFLURAMINE HYDROCHLORIDE"
],
"leaflet_url": null,
"authorised_at": "2020/12/18",
"procedure_number": "EMEA/H/C/003933",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/20/1491",
"additional_monitoring": "N"
}See everything about fenfluramine.
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.