Denmark· DK-28104113007
Imukin
A interferon gamma product containing interferon gamma-1b, human biosyntetisk, registered in Denmark by Orifarm A/S. The same ATC class is registered in 7 of our 19 countries.
Checked against Danish Medicines Agency (Denmark) on
Informational only — not a medical device.
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: Denmark, from Danish Medicines Agency (Denmark)
- 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
The record
At a glance
Danish Medicines Agency (Denmark)- Active substance
- INTERFERON GAMMA-1B, HUMAN BIOSYNTETISK
- Manufacturer
- Orifarm A/S
- Country
- Denmark (DK)
- ATC code
- L03AB03
- ATC class
- Interferon gamma
- Defined daily dose
- 40 mcg, P
- Reimbursed
- Not published by this register
- Source register
- Danish Medicines Agency (Denmark)
- Last checked
- September 30, 2026
Packs & prices · 1
- dk_varenummer28104113007
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under L03AB03
Interferon gamma, as other registers publish it.
- United KingdomImmukin 100micrograms/0.5ml solution for injection vialsClinigen Healthcare Ltd
- BelgiumImmukine 0,10 mgHorizon Pharma Ireland
- NetherlandsIMMUKINE, oplossing voor injectie 2 x 10.6 IE (0,1 mg)Clinigen Healthcare B.V.
- FinlandImukinBoehringer Ingelheim International GmbH
- NorwayImukinClinigen
- NorwayImukinClinigen Healthcare B.V.
- SwitzerlandImukin, InjektionslösungCuratis AG
- SwitzerlandImukin, InjektionslösungCuratis AG
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/99b3688e-6e6d-4094-a20a-fe0491303829 GET /v1/drugs/99b3688e-6e6d-4094-a20a-fe0491303829?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, opløsning",
"source": "dkma",
"strength": "200 mikrogram/ml",
"auth_role": "DKMA",
"dk_drugid": "28104113007",
"substance": "INTERFERON GAMMA-1B, HUMAN BIOSYNTETISK",
"auth_procedure": "Par-Imp",
"in_medicinpriser": true,
"registration_date_serial": "39324"
}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.