Ireland· IE-PA-PA25279/001/001
Zibor 2,500 IU anti Xa/0.2 ml solution for injection in pre-filled syringes
A bemiparin product containing bemiparin sodium, registered in Ireland by Gineladius S.L.. The same ATC class is registered in 4 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Bemiparin is registered in 4 of 19 countries.
Countries holding a registration under ATC B01AB12 (bemiparin), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 2 of them publish a price we can compare per daily dose
Bemiparin · ATC B01AB12
4 / 19 countries
- Czechiaprice
- Ireland
- Polandprice
- United Kingdom
The record
At a glance
HPRA (Ireland)- Active substance
- Bemiparin sodium
- Manufacturer
- Gineladius S.L.
- Country
- Ireland (IE)
- ATC code
- B01AB12
- ATC class
- Bemiparin
- Defined daily dose
- 2.5 TSD, E
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA25279/001/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Bemiparin in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Austria · Ivor, Ivorat
- Bulgaria · Зибор
- Czechia · Zibor
- Estonia · Zibor, Zibor 1000 Rü (Anti-Faktor Xa) 0,4 Ml Süstel
- Spain · Entervit, Hibor
- United Kingdom (Northern Ireland) · Zibor
- Greece · Ivor, Ivormax
- Hungary · Zibor
- Italy · Ivor
- Lithuania · Zibor
- Latvia · Zibor
- Poland · Zibor
- Portugal · Ivor
- Romania · Zibor
- Slovenia · Zibor
- Slovakia · Zibor
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/1c6327e1-661b-4c42-91f6-9c83aaf6711d GET /v1/drugs/1c6327e1-661b-4c42-91f6-9c83aaf6711d?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": "Solution for injection in pre-filled syringe",
"routes": [
"Subcutaneous use"
],
"source": "hpra",
"atc_all": [
"B01AB12"
],
"strength": null,
"pa_number": "PA25279/001/001",
"substances": [
"Bemiparin sodium"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Marketed",
"authorised_at": "03/05/2002",
"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 bemiparin.
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.