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France· FR:60074795

OCTAPLASLG, solution pour perfusion

A medicinal product containing protéines plasmatiques humaines, registered in France by OCTAPHARMA FRANCE.

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…normalisedOCTAPLASLG, solution pour perfusionATC—REGISTER NO.FR:60074795PACKS LISTED8CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
PROTÉINES PLASMATIQUES HUMAINES
Manufacturer
OCTAPHARMA FRANCE
Country
France (FR)
ATC code
—
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 8

  • cip13
    3400955003090
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin A ( abrogée le 07/01/2025)
  • cip13
    3400955003106
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin AB ( abrogée le 07/01/2025)
  • cip13
    3400955003113
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin B ( abrogée le 07/01/2025)
  • cip13
    3400955071969
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin A
  • cip13
    3400955071976
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin AB
  • cip13
    3400955071990
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin B
  • cip13
    3400955003120
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin O ( abrogée le 07/01/2025)
  • cip13
    3400955072003
    10 poche(s) PVC suremballée(s)/surpochée(s) de 200 ml. Groupe sanguin O

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/af63a080-02b8-4e80-95c8-9ef49e097989
GET /v1/drugs/af63a080-02b8-4e80-95c8-9ef49e097989?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": "60074795",
  "date_amm": "2016-02-02",
  "type_amm": "Procédure de reconnaissance mutuelle",
  "numero_ue": null,
  "substance": "PROTÉINES PLASMATIQUES HUMAINES",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution pour perfusion",
  "voies_administration": "intraveineuse",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about protéines plasmatiques humaines.

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.