Iceland· IS-EU/1/20/1495/004
Palforzia
A nahrungsmittel product containing arachis hypogaea allergens, registered in Iceland by STALLERGENES. The same ATC class is registered in 9 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Nahrungsmittel is registered in 9 of 19 countries.
Countries holding a registration under ATC V01AA08 (nahrungsmittel), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 6 of them publish a price we can compare per daily dose
Nahrungsmittel · ATC V01AA08
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- Switzerlandprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Arachis Hypogaea Allergens
- Manufacturer
- STALLERGENES
- Country
- Iceland (IS)
- ATC code
- V01AA08
- ATC class
- Nahrungsmittel
- 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 class
Other records under V01AA08
Nahrungsmittel, as other registers publish it.
- NetherlandsBencard Priktestoplossing "Voedingsmiddelen", oplossing voor huidpriktest 10.000 DU/mlAllergy Therapeutics Ibérica S.L.U.
- PolandPalforziaStallergenes
- DenmarkPalforziaAimmune Therapeutics Ireland Limited
- PolandPalforziaStallergenes
- PolandPalforziaStallergenes
- DenmarkPalforziaAimmune Therapeutics Ireland Limited
- PolandPalforziaStallergenes
- DenmarkPalforziaAimmune Therapeutics Ireland Limited
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/fd125c97-4b76-4d42-88e7-ffb656969eef GET /v1/drugs/fd125c97-4b76-4d42-88e7-ffb656969eef?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": "Duft til inntöku",
"source": "lyfjastofnun",
"atc_raw": "V01AA08",
"marketed": false,
"strength": "10 mg",
"ma_number": "EU/1/20/1495/004",
"substance": "Arachis Hypogaea Allergens",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í ofnæmis- og ónæmislækningum.\r\nMarkaðssetning á Íslandi er háð því að Lyfjastofnun hafi staðfest að sérstök skilyrði er varða öryggi og verkun við notkun lyfsins séu uppfyllt.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "44182"
}See everything about nahrungsmittel.
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.