Back to search

France· FR:68906518

ZILBRYSQ 16,6 mg, solution injectable en seringue préremplie

A zilucoplan product containing zilucoplan sodique, registered in France by UCB PHARMA BELGIQUE, on the national reimbursement list. The same ATC class is registered in 13 of our 19 countries.

Reimbursed in France (Assurance maladie)ATC L04AJ06

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…normalisedZILBRYSQ 16,6 mg, solution injectable…ATCL04AJ06REGISTER NO.FR:68906518PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Zilucoplan is registered in 13 of 19 countries.

Countries holding a registration under ATC L04AJ06 (zilucoplan), each read from that country’s own register.

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

Zilucoplan · ATC L04AJ06

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • 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
ZILUCOPLAN SODIQUE
Manufacturer
UCB PHARMA BELGIQUE
Country
France (FR)
ATC code
L04AJ06
ATC class
Zilucoplan
Defined daily dose
23 mg, P
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • cip13
    3400930280898
    7 seringues préremplies en verre avec dispositif de sécurité de 0,416 mL
    EUR 3.91

Regulatory notes

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

Same medicine, other countries

Zilucoplan in 13 other countries

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

All zilucoplan products

Authorised across Europe · EMA

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

  • Iceland · Zilbrysq
  • Liechtenstein · Zilbrysq
  • Norway · Zilbrysq

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/80dacc38-2608-41f0-b02c-69ad9d4a8fc4
GET /v1/drugs/80dacc38-2608-41f0-b02c-69ad9d4a8fc4?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": "68906518",
  "date_amm": "2023-12-01",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/23/1764",
  "substance": "ZILUCOPLAN SODIQUE",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution injectable",
  "voies_administration": "sous-cutanée",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Oui"
}

See everything about zilucoplan.

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.