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Ireland· IE-PA-PA2219/008/002

Wilate, 1000 IU VWF/1000 IU FVIII, powder and solvent for solution for injection

A von willebrand-faktor und faktor viii in kombination product containing human factor viii + von willebrand factor human, registered in Ireland by Octapharma (IP). The same ATC class is registered in 11 of our 19 countries.

ATC B02BD06

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedWilate, 1000 IU VWF/1000 IU FVIII, po…ATCB02BD06REGISTER NO.IE-PA-PA2219/008/002PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Von willebrand-faktor und faktor viii in kombination is registered in 11 of 19 countries.

Countries holding a registration under ATC B02BD06 (von willebrand-faktor und faktor viii in kombination), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 7 of them publish a price we can compare per daily dose

Von willebrand-faktor und faktor viii in kombination · ATC B02BD06

11 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
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

HPRA (Ireland)
Active substance
Human factor viii + Von willebrand factor human
Manufacturer
Octapharma (IP)
Country
Ireland (IE)
ATC code
B02BD06
ATC class
von Willebrand-Faktor und Faktor VIII in Kombination
Defined daily dose
1 TSD, E
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA2219/008/002

Regulatory notes

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

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/ea85b34d-4994-4197-83e1-a791a600f77d
GET /v1/drugs/ea85b34d-4994-4197-83e1-a791a600f77d?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": "Powder and solvent for solution for injection",
  "routes": [
    "Intravenous use"
  ],
  "source": "hpra",
  "atc_all": [
    "B02BD",
    "B02BD06"
  ],
  "strength": null,
  "pa_number": "PA2219/008/002",
  "substances": [
    "Human factor viii",
    "Von willebrand factor human"
  ],
  "legal_basis": "New active substance (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Marketed",
  "authorised_at": "16/03/2012",
  "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 von willebrand-faktor und faktor viii in kombination.

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.