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France· FR:67263268

ALTUVOCT 250 UI, poudre et solvant pour solution injectable

A efanesoctocog alfa product containing éfanésoctocog alfa, registered in France by SWEDISH ORPHAN BIOVITRUM (SUEDE). The same ATC class is registered in 2 of our 19 countries.

ATC B02BD45

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…normalisedALTUVOCT 250 UI, poudre et solvant po…ATCB02BD45REGISTER NO.FR:67263268PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Efanesoctocog alfa is registered in 2 of 19 countries.

Countries holding a registration under ATC B02BD45 (efanesoctocog alfa), each read from that country’s own register.

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

Efanesoctocog alfa · ATC B02BD45

2 / 19 countries

  • Franceprice
  • United Kingdom
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
ÉFANÉSOCTOCOG ALFA
Manufacturer
SWEDISH ORPHAN BIOVITRUM (SUEDE)
Country
France (FR)
ATC code
B02BD45
ATC class
Efanesoctocog alfa
Defined daily dose
500 E, P
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400930297230
    1 flacon en verre de 250 UI + 1 seringue préremplie en verre de 3 mL + 1 tige de piston + 1 adaptateur pour flacon + 1 set de perfusion

Regulatory notes

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

Same medicine, other countries

Efanesoctocog alfa in 13 other countries

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

All efanesoctocog alfa products

Authorised across Europe · EMA

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

  • Iceland · Altuvoct
  • Liechtenstein · Altuvoct
  • Norway · Altuvoct

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 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/dbff865a-07ee-45af-833e-92997ac88d85
GET /v1/drugs/dbff865a-07ee-45af-833e-92997ac88d85?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": "67263268",
  "date_amm": "2024-06-17",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/24/1824",
  "substance": "ÉFANÉSOCTOCOG ALFA",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "poudre et  solvant pour solution injectable",
  "voies_administration": "intraveineuse",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Oui"
}

See everything about efanesoctocog alfa.

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.