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Denmark· DK-28101867496

Febrivac PBE Vet.

A minkin enteriittivirus - / parvovirus - + inaktivoitu klostridirokote + inaktivoitu pseudomonas -rok product, registered in Denmark by CZ Vaccines S.A.U.,. The same ATC class is registered in 2 of our 19 countries.

ATC QI20CL01

Checked against Danish Medicines Agency (Denmark) on

Informational only — not a medical device.

SOURCE REGISTER · DKDanish Medicines Agency (Denmark)normalisedFebrivac PBE Vet.ATCQI20CL01REGISTER NO.DK-28101867496PACKS LISTED1CHECKEDSeptember 30, 2026

Where it is registered

Febrivac is registered in 2 of 19 countries.

Countries holding a registration under ATC QI20CL01 (minkin enteriittivirus - / parvovirus - + inaktivoitu klostridirokote + inaktivoitu pseudomonas -rok), each read from that country’s own register.

  • This record: Denmark, from Danish Medicines Agency (Denmark)
  • 1 of them publish a price we can compare per daily dose

Febrivac · ATC QI20CL01

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

Danish Medicines Agency (Denmark)
Manufacturer
CZ Vaccines S.A.U.,
Country
Denmark (DK)
ATC code
QI20CL01
ATC class
Minkin enteriittivirus - / parvovirus - + Inaktivoitu Klostridirokote + Inaktivoitu Pseudomonas -rok
Reimbursed
Not published by this register
Source register
Danish Medicines Agency (Denmark)
Last checked
September 30, 2026

Packs & prices · 1

  • dk_varenummer
    28101867496

Regulatory notes

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

Same class

Other records under QI20CL01

Minkin enteriittivirus - / parvovirus - + inaktivoitu klostridirokote + inaktivoitu pseudomonas -rok, as other registers publish it.

All Febrivac products

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Danish Medicines Agency (Denmark). 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/7cbbca6d-774f-41b8-a90e-19495942a152
GET /v1/drugs/7cbbca6d-774f-41b8-a90e-19495942a152?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": "injektionsvæske, suspension",
  "source": "dkma",
  "strength": "6532",
  "auth_role": "DKMA",
  "dk_drugid": "28101867496",
  "substance": null,
  "auth_procedure": "National",
  "in_medicinpriser": false,
  "registration_date_serial": "36950"
}

See everything about Febrivac.

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.