Iceland· IS-EU/1/24/1866/001

ELAHERE

A mirvetuximab soravtansine product containing mirvetuximab soravtansine, registered in Iceland by AbbVie Deutschland GmbH & Co. KG. The same ATC class is registered in 13 of our 19 countries.

ATC L01FX26

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedELAHEREATCL01FX26REGISTER NO.IS-EU/1/24/1866/001PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Mirvetuximab soravtansine is registered in 13 of 19 countries.

Countries holding a registration under ATC L01FX26 (mirvetuximab soravtansine), 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

Mirvetuximab soravtansine · ATC L01FX26

13 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • 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
Mirvetuximab soravtansine
Manufacturer
AbbVie Deutschland GmbH & Co. KG
Country
Iceland (IS)
ATC code
L01FX26
ATC class
Mirvetuximab soravtansine
Defined daily dose
18 mg, 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.

Same medicine, other countries

Mirvetuximab soravtansine in 13 other countries

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

All mirvetuximab soravtansine products

Authorised across Europe · EMA

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

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

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/043cd0cd-ff23-4691-b84b-6b71872ed556
GET /v1/drugs/043cd0cd-ff23-4691-b84b-6b71872ed556?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": "Innrennslisþykkni, lausn",
  "source": "lyfjastofnun",
  "atc_raw": "L01FX26",
  "marketed": false,
  "strength": "5 mg/ml",
  "ma_number": "EU/1/24/1866/001",
  "substance": "Mirvetuximab soravtansine",
  "other_info": null,
  "legal_status": "(R) Lyfseðilsskylt\r\n(H) Sjúkrahúsmerkt",
  "ma_issued_serial": "45610"
}

See everything about mirvetuximab soravtansine.

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.