Iceland· IS-EU/1/16/1155/001-002

Kyntheum

A brodalumab product containing brodalumabum inn, registered in Iceland by LEO Pharma A/S*. The same ATC class is registered in 13 of our 19 countries.

ATC L04AC12

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedKyntheumATCL04AC12REGISTER NO.IS-EU/1/16/1155/001-0…PACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Brodalumab is registered in 13 of 19 countries.

Countries holding a registration under ATC L04AC12 (brodalumab), 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

Brodalumab · ATC L04AC12

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • 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
Brodalumabum INN
Manufacturer
LEO Pharma A/S*
Country
Iceland (IS)
ATC code
L04AC12
ATC class
Brodalumab
Defined daily dose
15 mg, P
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 2026

Packs & prices · 1

1 priced
  • ean
    588134
    1,5 ml x2 áf.spr
    ISK 196779

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

59 interactions on record for brodalumab.

Graded by severity as the source publishes them — 27 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

Brodalumab · interactions on record

59 records

  • 27 severe
  • 25 moderate
  • 7 minor

Most severe, free to view

  • CladribineL01BB04severe
  • Talimogene laherparepvecL01XL02severe
  • Talimogen laherparepvecL01XX51severe
  • LeflunomidL04AA13severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Brodalumab in 14 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All brodalumab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Kyntheum
  • Liechtenstein · Kyntheum
  • Norway · Kyntheum

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/2301ca3c-f9ff-410b-9a80-c4d99348a871
GET /v1/drugs/2301ca3c-f9ff-410b-9a80-c4d99348a871?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 áfylltri sprautu",
  "source": "lyfjastofnun",
  "atc_raw": "L04AC12",
  "marketed": true,
  "strength": "210 mg",
  "ma_number": "EU/1/16/1155/001-002",
  "substance": "Brodalumabum INN",
  "other_info": "Ávísun lyfsins er bundin við sérfræðinga í gigtarlækningum, húðsjúkdómum og ónæmisfræði.",
  "legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
  "ma_issued_serial": "42933"
}

See everything about brodalumab.

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.