Denmark· DK-28107597526
Fobuler
A formoterol and budesonide product containing budesonid, formoterolfumarat dihydrat, registered in Denmark by Orifarm A/S. The same ATC class is registered in 14 of our 19 countries.
Checked against Danish Medicines Agency (Denmark) on
Informational only — not a medical device.
Where it is registered
Formoterol and budesonide is registered in 14 of 19 countries.
Countries holding a registration under ATC R03AK07 (formoterol and budesonide), each read from that country’s own register.
- This record: Denmark, from Danish Medicines Agency (Denmark)
- 9 of them publish a price we can compare per daily dose
Formoterol and budesonide · ATC R03AK07
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Danish Medicines Agency (Denmark)- Active substance
- BUDESONID, FORMOTEROLFUMARAT DIHYDRAT
- Manufacturer
- Orifarm A/S
- Country
- Denmark (DK)
- ATC code
- R03AK07
- ATC class
- Formoterol and budesonide
- Defined daily dose
- 24 mcg, Inhal
- Reimbursed
- Not published by this register
- Source register
- Danish Medicines Agency (Denmark)
- Last checked
- September 30, 2026
Packs & prices · 1
- dk_varenummer28107597526
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under R03AK07
Formoterol and budesonide, as other registers publish it.
- FinlandAerocomp ForspiroSandoz A/S
- FinlandAerocomp ForspiroSandoz A/S
- PolandAirbufo ForspiroSandoz GmbH
- PolandAirbufo ForspiroSandoz GmbH
- CzechiaAIRBUFO FORSPIROSandoz s.r.o., Praha
- CzechiaAIRBUFO FORSPIROSandoz s.r.o., Praha
- CzechiaAIRBUFO FORSPIROSandoz s.r.o., Praha
- CzechiaAIRBUFO FORSPIROSandoz s.r.o., Praha
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/f1a32657-601b-4cb1-ad1a-ba0558063920 GET /v1/drugs/f1a32657-601b-4cb1-ad1a-ba0558063920?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": "inhalationspulver",
"source": "dkma",
"strength": "9+320 mikrog/dosis",
"auth_role": "DKMA",
"dk_drugid": "28107597526",
"substance": "BUDESONID, FORMOTEROLFUMARAT DIHYDRAT",
"auth_procedure": "Par-Imp",
"in_medicinpriser": false,
"registration_date_serial": "46184"
}See everything about formoterol and budesonide.
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.