Iceland· IS-EU/1/25/1977/001-003
Zurzuvae
A zuranolone product containing zuranolone, registered in Iceland by Biogen Netherlands B.V.. The same ATC class is registered in 8 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Zuranolone is registered in 8 of 19 countries.
Countries holding a registration under ATC N06AX31 (zuranolone), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 5 of them publish a price we can compare per daily dose
Zuranolone · ATC N06AX31
8 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Zuranolone
- Manufacturer
- Biogen Netherlands B.V.
- Country
- Iceland (IS)
- ATC code
- N06AX31
- ATC class
- Zuranolone
- 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
Zuranolone in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaZURZUVAEBiogen Netherlands B.V., Badhoevedorp
- United StatesZURZUVAEBiogen MA Inc.
- IrelandZurzuvae 20 mg hard capsulesBiogen Netherlands B.V.
- BelgiumZurzuvae 20 mgBiogen Netherlands
- PolandZurzuvaeBiogen Netherlands B.V.
- SwedenZurzuvae 20 mg Kapsel, hårdBiogen Netherlands B.V.
- NetherlandsZurzuvae 20 mg harde capsulesBiogen Netherlands B.V.
- FinlandZurzuvaeBiogen Netherlands B.V.
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Liechtenstein · Zurzuvae
- Norway · Zurzuvae
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 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/08636650-5281-4f95-af46-426ab062f0c3 GET /v1/drugs/08636650-5281-4f95-af46-426ab062f0c3?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": "Hart hylki",
"source": "lyfjastofnun",
"atc_raw": "N06AX31",
"marketed": false,
"strength": "20 mg",
"ma_number": "EU/1/25/1977/001-003",
"substance": "Zuranolone",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "45917"
}See everything about zuranolone.
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.