Iceland· IS-EU/1/16/1157/001-002 & 005

Suliqua

A insulin glargine and lixisenatide product containing insulinum glarginum inn,lixisenatidum inn,lixisenatidum inn, registered in Iceland by Sanofi Winthrop Industrie. The same ATC class is registered in 10 of our 19 countries.

ATC A10AE54

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedSuliquaATCA10AE54REGISTER NO.IS-EU/1/16/1157/001-0…PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Insulin glargine and lixisenatide is registered in 10 of 19 countries.

Countries holding a registration under ATC A10AE54 (insulin glargine and lixisenatide), 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

Insulin glargine and lixisenatide · ATC A10AE54

10 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Netherlands
  • Polandprice
  • 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
Insulinum glarginum INN,Lixisenatidum INN,Lixisenatidum INN
Manufacturer
Sanofi Winthrop Industrie
Country
Iceland (IS)
ATC code
A10AE54
ATC class
Insulin glargine and lixisenatide
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/5990401f-0f89-41be-a4e4-ccbb9a33d6ad
GET /v1/drugs/5990401f-0f89-41be-a4e4-ccbb9a33d6ad?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": "A10AE54",
  "marketed": false,
  "strength": "100 ein./ml + 50 míkróg/ml",
  "ma_number": "EU/1/16/1157/001-002 & 005",
  "substance": "Insulinum glarginum INN,Lixisenatidum INN,Lixisenatidum 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": "42746"
}

See everything about insulin glargine and lixisenatide.

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.