Finland· FI-REL-REL3444

Imukin

A interferon gamma product containing interferon gamma 2a, registered in Finland by Boehringer Ingelheim International GmbH. The same ATC class is registered in 7 of our 19 countries.

ATC L03AB03

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedImukinATCL03AB03REGISTER NO.FI-REL-REL3444PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Interferon gamma is registered in 7 of 19 countries.

Countries holding a registration under ATC L03AB03 (interferon gamma), each read from that country’s own register.

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

Interferon gamma · ATC L03AB03

7 / 19 countries

  • Belgiumprice
  • Denmark
  • Finlandprice
  • Netherlands
  • Norwayprice
  • Switzerlandprice
  • United Kingdom
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
Interferon gamma 2a
Manufacturer
Boehringer Ingelheim International GmbH
Country
Finland (FI)
ATC code
L03AB03
ATC class
Interferon gamma
Defined daily dose
40 mcg, P
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.

Same medicine, other countries

Interferon gamma in 7 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All interferon gamma products

Authorised across Europe · EMA

The same active substance is authorised in 6 EEA countries. Names it is sold under:

  • Germany · Imukin
  • Spain · Imukin
  • France · Imukin
  • United Kingdom (Northern Ireland) · Immukin
  • Italy · Imukin
  • Netherlands · Immukine

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 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/27134b14-837f-4347-ac0f-97791d385481
GET /v1/drugs/27134b14-837f-4347-ac0f-97791d385481?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": "40",
  "form": "injektioneste, liuos",
  "route": null,
  "ddd_unit": "mcg",
  "strength": "0.2 mg/ml",
  "atc_label": "interferoni gamma",
  "ma_number": "11404",
  "auth_status": "Myyntilupa peruuntunut",
  "eu_ma_number": null,
  "fimea_rel_id": "REL3444",
  "authorised_at": "1994-03-07"
}

See everything about interferon gamma.

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.