Iceland· IS-EU/1/19/1408/006-010
Sunosi
A solriamfetol product containing solriamfetolum inn hýdróklóríð, registered in Iceland by Atnahs Pharma Netherlands B.V.. The same ATC class is registered in 14 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Solriamfetol is registered in 14 of 19 countries.
Countries holding a registration under ATC N06BA14 (solriamfetol), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 9 of them publish a price we can compare per daily dose
Solriamfetol · ATC N06BA14
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of solriamfetol costs, country by country.
Normalised to the WHO defined daily dose (0.1 g), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Solriamfetol · price per daily dose (0.1 g)
USD · FX 28 Sept 2026
- FR France$10.89
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Solriamfetolum INN hýdróklóríð
- Manufacturer
- Atnahs Pharma Netherlands B.V.
- Country
- Iceland (IS)
- ATC code
- N06BA14
- ATC class
- Solriamfetol
- Defined daily dose
- 0.1 g, O
- 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.
Interactions
54 interactions on record for solriamfetol.
Graded by severity as the source publishes them — 4 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Solriamfetol · interactions on record
54 records
- 4 severe
- 50 moderate
Most severe, free to view
- ProcarbazineL01XB01severe
- OzanimodL04AA38severe
- OzanimodL04AE02severe
- Methylthioninium chlorideV03AB17severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Solriamfetol in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaSUNOSIAtnahs Pharma Netherlands B.V., Amsterdam
- FinlandSunosiParanova Oy
- SpainSUNOSI 150 mg COMPRIMIDOS RECUBIERTOS CON PELICULAAtnahs Pharma Netherlands Bv.
- FranceSUNOSI 150 mg, comprimé pelliculéATNAHS PHARMA NETHERLANDS (PAYS-BAS)
- IrelandSunosi 150 mg film-coated tabletsAtnahs Pharma Netherlands B.V.
- NetherlandsSunosi 150 mg filmomhulde tablettenAtnahs Pharma Netherlands B.V.
- NorwaySunosiAtnahs Pharma Netherlands B.V.
- PolandSunosiAtnahs Pharma Netherlands B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Sunosi
- Liechtenstein · Sunosi
- Norway · Sunosi
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/f71fed84-0cc8-49ea-ad40-f8bbfce138e4 GET /v1/drugs/f71fed84-0cc8-49ea-ad40-f8bbfce138e4?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": "Filmuhúðuð tafla",
"source": "lyfjastofnun",
"atc_raw": "N06BA14",
"marketed": false,
"strength": "150 mg",
"ma_number": "EU/1/19/1408/006-010",
"substance": "Solriamfetolum INN hýdróklóríð",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í geðlækningum, taugalækningum og lungnalækningum.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "43846"
}See everything about solriamfetol.
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.