France· FR:67884271
SONOVUE 8 microlitres par ml, poudre et solvant pour dispersion injectable
A medicinal product containing soufre (hexafluorure de), registered in France by BRACCO INTERNATIONAL, on the national reimbursement list.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- SOUFRE (HEXAFLUORURE DE)
- Manufacturer
- BRACCO INTERNATIONAL
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip1334009357564661 flacon(s) en verre de 25 mg - 1 seringue(s) préremplie(s) en verre de 5 ml avec dispositif de transfert Mini-SpikeEUR 65.84
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Soufre (hexafluorure de) in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandSonovueBracco International B.V.
- CanadaSONOVUEBRACCO IMAGING CANADA
- SwitzerlandSonoVue 8 µL/mL, polvere e solvente per dispersione iniettabileBracco Suisse SA
- CzechiaSONOVUEBracco International B.V., Amsterdam
- SpainSONOVUE 8 MICROLITROS/ml POLVO Y DISOLVENTE PARA DISPERSION INYECTABLEBracco International B.V.
- United KingdomSonoVue 8microlitres/ml powder and solvent for dispersion for injection vialsBracco UK Ltd
- IrelandSonoVue 8 microlitres/mL powder and solvent for dispersion for injectionBracco International B.V.
- IcelandSonoVueBracco International B.V.*
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/91b19d54-57e6-4f51-b656-4227ea39182b GET /v1/drugs/91b19d54-57e6-4f51-b656-4227ea39182b?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": "67884271",
"date_amm": "2001-03-26",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/01/177",
"substance": "SOUFRE (HEXAFLUORURE DE)",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "poudre et solvant pour dispersion injectable",
"voies_administration": "intraveineuse;intravésicale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about soufre (hexafluorure de).
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.