Iceland· IS-EU/1/25/2001/001-002
Dawnzera
A donidalorsen product containing donidalorsen sodium, registered in Iceland by Otsuka Pharmaceutical Netherlands B.V.*. The same ATC class is registered in 10 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Donidalorsen is registered in 10 of 19 countries.
Countries holding a registration under ATC B06AC09 (donidalorsen), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 8 of them publish a price we can compare per daily dose
Donidalorsen · ATC B06AC09
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Norwayprice
- Spainprice
- Switzerlandprice
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Donidalorsen sodium
- Manufacturer
- Otsuka Pharmaceutical Netherlands B.V.*
- Country
- Iceland (IS)
- ATC code
- B06AC09
- ATC class
- Donidalorsen
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 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
Donidalorsen in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaDAWNZERAOtsuka Pharmaceutical Netherlands B.V., Amsterdam
- BelgiumDawnzera 80 mgOtsuka Pharmaceutical Netherlands
- FinlandDawnzeraOtsuka Pharmaceutical Netherlands B.V.
- IrelandDawnzera 80mg solution for injection in pre-filled penOtsuka Pharmaceutical Netherlands B.V.
- United StatesDAWNZERAIonis Pharmaceuticals Inc.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Icelandic Medicines Agency (Iceland). 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/2adbe6f3-abce-4da4-8f04-7c068e6ff808 GET /v1/drugs/2adbe6f3-abce-4da4-8f04-7c068e6ff808?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": "Stungulyf, lausn í áfylltum lyfjapenna",
"source": "lyfjastofnun",
"atc_raw": "B06AC09",
"marketed": false,
"strength": "80 mg",
"ma_number": "EU/1/25/2001/001-002",
"substance": "Donidalorsen sodium",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í ofnæmis- og ónæmislækningum.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "46041"
}See everything about donidalorsen.
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.