Iceland· IS-EU/1/14/947/001-004

Xultophy

A insulin degludec and liraglutide product containing liraglutidum inn,insulinum degludecum inn, registered in Iceland by Novo Nordisk A/S*. The same ATC class is registered in 12 of our 19 countries.

ATC A10AE56

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedXultophyATCA10AE56REGISTER NO.IS-EU/1/14/947/001-004PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Insulin degludec and liraglutide is registered in 12 of 19 countries.

Countries holding a registration under ATC A10AE56 (insulin degludec and liraglutide), 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

Insulin degludec and liraglutide · ATC A10AE56

12 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

Icelandic Medicines Agency (Iceland)
Active substance
Liraglutidum INN,Insulinum degludecum INN
Manufacturer
Novo Nordisk A/S*
Country
Iceland (IS)
ATC code
A10AE56
ATC class
Insulin degludec and liraglutide
Defined daily dose
40 E, P
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.

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/e0e4d91c-009d-4626-a0b3-dafa172aa748
GET /v1/drugs/e0e4d91c-009d-4626-a0b3-dafa172aa748?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": "A10AE56",
  "marketed": false,
  "strength": "100 ein./ml +3,6 mg/ml",
  "ma_number": "EU/1/14/947/001-004",
  "substance": "Liraglutidum INN,Insulinum degludecum INN",
  "other_info": "Markaðssetning 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) Lyfseðilsskylt",
  "ma_issued_serial": "41900"
}

See everything about insulin degludec and liraglutide.

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.