Germany· DE-A57-b90e553f3bf1d76b

Curosurf

A medicinal product containing poractant alfa, registered in Germany by Chiesi Gmbh.

Checked against EMA Article 57 (European Union) on

Informational only — not a medical device.

SOURCE REGISTER · DEEMA Article 57 (European Union)normalisedCurosurfATC—REGISTER NO.DE-A57-b90e553f3bf1d7…PACKS LISTED0CHECKEDJuly 8, 2026

The record

At a glance

EMA Article 57 (European Union)
Active substance
Poractant Alfa
Manufacturer
Chiesi Gmbh
Country
Germany (DE)
ATC code
—
Reimbursed
Not published by this register
Source register
EMA Article 57 (European Union)
Last checked
July 8, 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

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 29 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
  • France · 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 EMA Article 57 (European Union). 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/764117f0-1124-4eda-b7f7-8b4f09ad3e3d
GET /v1/drugs/764117f0-1124-4eda-b7f7-8b4f09ad3e3d?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.

{
  "pzn": null,
  "route": "Endotracheopulmonary Use",
  "source": "ema_art57_de",
  "ma_number": null,
  "substance": "Poractant Alfa",
  "atc_from_source": null,
  "authorisation_country": "Germany"
}

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.