Ireland· IE-PA-PA0776/002/003
Clopixol 10mg Film-coated Tablets
A zuclopenthixol product containing zuclopenthixol hydrochloride, registered in Ireland by Lundbeck ( Ireland ) Limited. The same ATC class is registered in 14 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Zuclopenthixol is registered in 14 of 19 countries.
Countries holding a registration under ATC N05AF05 (zuclopenthixol), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 8 of them publish a price we can compare per daily dose
Zuclopenthixol · ATC N05AF05
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
Price per daily dose
What a daily dose of zuclopenthixol costs, country by country.
Normalised to the WHO defined daily dose (30 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
Zuclopenthixol · price per daily dose (30 mg)
USD · FX 28 Sept 2026
- CH Switzerland$1.27
The record
At a glance
HPRA (Ireland)- Active substance
- Zuclopenthixol hydrochloride
- Manufacturer
- Lundbeck ( Ireland ) Limited
- Country
- Ireland (IE)
- ATC code
- N05AF05
- ATC class
- Zuclopenthixol
- Defined daily dose
- 30 mg, O
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA0776/002/003
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
70 interactions on record for zuclopenthixol.
Mechanism, severity and management for each pair, from a commercially licensed source — included 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
Zuclopenthixol · interactions on record
70 records
70 more interactions with mechanism and management, from a commercially licensed source.
Sign in to checkSame medicine, other countries
Zuclopenthixol in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsCisordinol 10 mg, filmomhulde tablettenMedcor Pharmaceuticals B.V.
- CzechiaCISORDINOLH. Lundbeck A/S, Valby
- SwedenCisordinol 10 mg Filmdragerad tablettH. Lundbeck A/S
- FranceCLOPIXOL 10 mg, comprimé pelliculéLUNDBECK SAS
- BelgiumClopixol 10 mgLundbeck
- NorwayCisordinolH. Lundbeck A/S
- PolandClopixolH. Lundbeck A/S
- IcelandCisordinolH. Lundbeck A/S*
Authorised across Europe · EMA
The same active substance is authorised in 26 EEA countries. Names it is sold under:
- Austria · Cisordinol, Cisordinol Acutard
- Belgium · Clopixol, Clopixol Acutard
- Bulgaria · Клопиксол, Клопиксол-Акюфейз
- Czechia · Cisordinol, Cisordinol-Acutard
- Germany · Ciatyl-Z, Ciatyl-Z Acuphase
- Denmark · Cisordinol, Cisordinol-Acutard
- Estonia · Cisordinol, Cisordinol-Acutard
- Spain · Clopixol, Clopixol Acufase
- Finland · Cisordinol, Cisordinol-Acutard
- France · Clopixol, Clopixol A Action Semi-Prolongee
- United Kingdom (Northern Ireland) · Clopixol, Clopixol-Acuphase
- Greece · Clopixol, Clopixol Acutard
- Hungary · Cisordinol, Cisordinol-Acutard
- Iceland · Cisordinol, Cisordinol-Acutard
- Italy · Clopixol
- Lithuania · Cisordinol, Cisordinol-Acutard
- Luxembourg · Clopixol, Clopixol Acutard
- Latvia · Cisordinol, Cisordinol-Acutard
- Netherlands · Cisordinol, Cisordinol-Acutard
- Norway · Cisordinol, Cisordinol-Acutard
- Poland · Clopixol, Clopixol Acuphase
- Portugal · Cisordinol Acutard
- Romania · Clopixol
- Sweden · Cisordinol, Cisordinol-Acutard
- Slovenia · Clopixol, Clopixol-Acuphase
- Slovakia · Cisordinol
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 HPRA (Ireland). 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/bff0b33d-1b36-48dc-8979-dca795b846db GET /v1/drugs/bff0b33d-1b36-48dc-8979-dca795b846db?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": "Film-coated tablet",
"routes": [
"Oral use"
],
"source": "hpra",
"atc_all": [
"N05AF",
"N05AF05"
],
"strength": null,
"pa_number": "PA0776/002/003",
"substances": [
"Zuclopenthixol hydrochloride"
],
"legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
"market_info": "Marketed",
"authorised_at": "01/11/1982",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about zuclopenthixol.
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.