Finland· FI-REL-REL43178

Eryseng Parvo

A inaktivoitu sian parvovirus -rokote + inaktivoitu erysipelothrix rokote product containing porcine parvovirus, inactivated + erysipelothrix rhusiopathiae bacterium, serotype 2, inactivated, registered in Finland by Laboratorios Hipra S.A.. The same ATC class is registered in 2 of our 19 countries.

ATC QI09AL01

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedEryseng ParvoATCQI09AL01REGISTER NO.FI-REL-REL43178PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Porcine parvovirus, inactivated + erysipelothrix rhusiopathiae bacterium, serotype 2, inactivated is registered in 2 of 19 countries.

Countries holding a registration under ATC QI09AL01 (inaktivoitu sian parvovirus -rokote + inaktivoitu erysipelothrix rokote), each read from that country’s own register.

  • This record: Finland, from Fimea (Finland)
  • 1 of them publish a price we can compare per daily dose

Porcine parvovirus, inactivated + erysipelothrix rhusiopathiae bacterium, serotype 2, inactivated · ATC QI09AL01

2 / 19 countries

  • Denmark
  • Finlandprice
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

Fimea (Finland)
Active substance
Porcine parvovirus, inactivated + Erysipelothrix rhusiopathiae bacterium, serotype 2, inactivated
Manufacturer
Laboratorios Hipra S.A.
Country
Finland (FI)
ATC code
QI09AL01
ATC class
Inaktivoitu sian parvovirus -rokote + inaktivoitu erysipelothrix rokote
Reimbursed
Not published by this register
Source register
Fimea (Finland)
Last checked
September 27, 2026

Packs & prices · 0

No packs listed by the register for this record.

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 Fimea (Finland). 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/4557c504-8384-4d6d-9a28-f0a4bcccd695
GET /v1/drugs/4557c504-8384-4d6d-9a28-f0a4bcccd695?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.

{
  "ddd": null,
  "form": "injektioneste, suspensio",
  "route": "Lihakseen",
  "ddd_unit": null,
  "strength": null,
  "atc_label": "Inaktivoitu sian parvovirus -rokote + inaktivoitu erysipelothrix rokote",
  "ma_number": null,
  "auth_status": "Myyntilupa myönnetty",
  "eu_ma_number": "EU/2/14/167/001-007",
  "fimea_rel_id": "REL43178",
  "authorised_at": "2014-07-08"
}

See everything about porcine parvovirus, inactivated + erysipelothrix rhusiopathiae bacterium, serotype 2, inactivated.

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.