Iceland· IS-EU/1/15/1056/001

Praxbind

A idarucizumab product containing idarucizumabum inn, registered in Iceland by Boehringer Ingelheim International GmbH*. The same ATC class is registered in 13 of our 19 countries.

ATC V03AB37

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedPraxbindATCV03AB37REGISTER NO.IS-EU/1/15/1056/001PACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Idarucizumab is registered in 13 of 19 countries.

Countries holding a registration under ATC V03AB37 (idarucizumab), 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

Idarucizumab · ATC V03AB37

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • 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
Idarucizumabum INN
Manufacturer
Boehringer Ingelheim International GmbH*
Country
Iceland (IS)
ATC code
V03AB37
ATC class
Idarucizumab
Defined daily dose
5 g, P
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 2026

Packs & prices · 1

1 priced
  • ean
    450413
    50 ml x2 hgl
    ISK 417401

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/4150f14c-cf85-43ff-9f98-2448a6e76c5e
GET /v1/drugs/4150f14c-cf85-43ff-9f98-2448a6e76c5e?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/innrennslislyf, lausn",
  "source": "lyfjastofnun",
  "atc_raw": "V03AB37",
  "marketed": true,
  "strength": "2,5 g/50 ml",
  "ma_number": "EU/1/15/1056/001",
  "substance": "Idarucizumabum INN",
  "other_info": null,
  "legal_status": "(R) Lyfseðilsskylt\r\n(H) Sjúkrahúsmerkt",
  "ma_issued_serial": "42328"
}

See everything about idarucizumab.

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.