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France· FR:61116813

ENFLONSIA 105 mg, solution injectable en seringue préremplie

A clesrovimab product containing clesrovimab, registered in France by MERCK SHARP & DOHME (PAYS-BAS), on the national reimbursement list. The same ATC class is registered in 11 of our 19 countries.

Reimbursed in France (Assurance maladie)ATC J06BD10

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…normalisedENFLONSIA 105 mg, solution injectable…ATCJ06BD10REGISTER NO.FR:61116813PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Clesrovimab is registered in 11 of 19 countries.

Countries holding a registration under ATC J06BD10 (clesrovimab), each read from that country’s own register.

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

Clesrovimab · ATC J06BD10

11 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • 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
CLESROVIMAB
Manufacturer
MERCK SHARP & DOHME (PAYS-BAS)
Country
France (FR)
ATC code
J06BD10
ATC class
Clesrovimab
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • cip13
    3400930328613
    1 seringue préremplie en verre de 0,7 mL + 1 aiguille
    EUR 401.8

Regulatory notes

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

Same medicine, other countries

Clesrovimab in 12 other countries

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

All clesrovimab products

Authorised across Europe · EMA

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

  • Iceland · Enflonsia
  • Liechtenstein · Enflonsia
  • Norway · Enflonsia

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/88f0ab70-eed7-4dd5-8be3-7295dbc4e4b2
GET /v1/drugs/88f0ab70-eed7-4dd5-8be3-7295dbc4e4b2?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": "61116813",
  "date_amm": "2026-04-15",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/25/1984",
  "substance": "CLESROVIMAB",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution injectable",
  "voies_administration": "intramusculaire",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Oui"
}

See everything about clesrovimab.

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.