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France· FR:64447081

CUROSURF 240 mg/3 ml, suspension pour instillation endotrachéobronchique

A medicinal product containing poractant alfa, registered in France by CHIESI.

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…normalisedCUROSURF 240 mg/3 ml, suspension pour…ATC—REGISTER NO.FR:64447081PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
PORACTANT ALFA
Manufacturer
CHIESI
Country
France (FR)
ATC code
—
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400955775379
    1 flacon(s) en verre de 3 ml

Regulatory notes

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

Same medicine, other countries

Poractant alfa in 9 other countries

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

All poractant alfa products

Authorised across Europe · EMA

The same active substance is authorised in 28 EEA countries. Names it is sold under:

  • Austria · Curosurf
  • Belgium · Curosurf
  • Bulgaria · Куросърф
  • Cyprus · Curosurf
  • Czechia · Curosurf
  • Denmark · Curosurf
  • Estonia · Curosurf
  • Spain · Curosurf
  • Finland · Curosurf
  • United Kingdom (Northern Ireland) · Curosurf
  • Greece · Curosurf
  • Croatia · Curosurf
  • Hungary · Curosurf
  • Ireland · Curosurf
  • Iceland · Curosurf
  • Italy · Curosurf
  • Lithuania · Curosurf
  • Luxembourg · Curosurf
  • Latvia · Curosurf
  • Malta · Curosurf
  • Netherlands · Curosurf
  • Norway · Curosurf
  • Poland · Curosurf
  • Portugal · Curosurf
  • Romania · Curosurf
  • Sweden · Curosurf
  • Slovenia · Curosurf
  • Slovakia · Curosurf

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/c5756058-6b68-46a7-9063-7d0d88b13874
GET /v1/drugs/c5756058-6b68-46a7-9063-7d0d88b13874?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": "64447081",
  "date_amm": "1992-08-06",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "PORACTANT ALFA",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "suspension pour instillation",
  "voies_administration": "endotrachéobronchique",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about poractant 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.