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France· FR:63288174

ELAPRASE 2 mg/ml, solution à diluer pour perfusion

A idursulfase product containing idursulfase, registered in France by TAKEDA PHARMACEUTICALS INTERNATIONAL (IRLANDE), on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.

Reimbursed in France (Assurance maladie)ATC A16AB09

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedELAPRASE 2 mg/ml, solution à diluer p…ATCA16AB09REGISTER NO.FR:63288174PACKS LISTED2CHECKEDSeptember 12, 2026

Where it is registered

Idursulfase is registered in 14 of 19 countries.

Countries holding a registration under ATC A16AB09 (idursulfase), each read from that country’s own register.

  • This record: France, from Base de données publique des médicaments — BDPM (France)
  • 9 of them publish a price we can compare per daily dose

Idursulfase · ATC A16AB09

14 / 19 countries

  • Belgiumprice
  • Canada
  • 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

Base de données publique des médicaments — BDPM (France)
Active substance
IDURSULFASE
Manufacturer
TAKEDA PHARMACEUTICALS INTERNATIONAL (IRLANDE)
Country
France (FR)
ATC code
A16AB09
ATC class
Idursulfase
Defined daily dose
5 mg, P
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 2

1 priced
  • cip13
    3400930236536
    1 flacon(s) en verre de 3 ml
    EUR 2.56
  • cip13
    3400957056339
    1 flacon(s) en verre de 3 ml ( abrogée le 02/05/2022)

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 Base de données publique des médicaments — BDPM (France). 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/c18dbca5-988a-4fc7-9358-076dcf820c7c
GET /v1/drugs/c18dbca5-988a-4fc7-9358-076dcf820c7c?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.

{
  "cis": "63288174",
  "date_amm": "2007-01-08",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/06/365",
  "substance": "IDURSULFASE",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution à diluer pour perfusion",
  "voies_administration": "intraveineuse",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Oui"
}

See everything about idursulfase.

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.