France· FR:68951171
ACTOSOLV 100 000 UI, poudre pour solution injectable/pour perfusion
A medicinal product, registered in France by EUMEDICA PHARMACEUTICALS (ALLEMAGNE).
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)- Manufacturer
- EUMEDICA PHARMACEUTICALS (ALLEMAGNE)
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- No
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
- cip1334009565106721 flacon(s) en verre de 100000 UI
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
ACTOSOLV in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomSyner-KINASE 10,000unit powder for solution for injection vialsSyner-Med (Pharmaceutical Products) Ltd
- NetherlandsUrokinase Pharma-Zentrale 10.000 IE, poeder voor oplossing voor intraveneuze infusiePharma-Zentrale GmbH
- BelgiumActosolv 100000 IUEumedica Pharmaceuticals
- SpainUROKINASE TEOFARMA 100.000 UI. POLVO Y DISOLVENTE PARA SOLUCION PARA PERFUSIONTeofarma S.R.L.
- PolandUrokinase medacPharma-Zentrale GmbH
- GermanyRheotrombEumedica / Belgium
- FinlandUrokinase MedacMedac Gesellschaft Für Klinische Spezialpräparate mbH
- Japanウロキナーゼ持田製薬
Authorised across Europe · EMA
The same active substance is authorised in 9 EEA countries. Names it is sold under:
- Austria · Urokinase Medac
- Belgium · Actosolv, Urokinase Syner-Medica
- Germany · Rheotromb, Syner-Kinase
- Spain · Urokinase Teofarma, Uroquinasa Syner Medica
- United Kingdom (Northern Ireland) · Syner-Kinase
- Italy · Urochinasi Eg, Urokinasi Pfizer
- Luxembourg · Actosolv
- Netherlands · Urokinase Devrimed, Urokinase Pharma-Zentrale
- Poland · Urokinase Medac
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/7b048a81-85ad-46aa-a792-e327e28dac8c GET /v1/drugs/7b048a81-85ad-46aa-a792-e327e28dac8c?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": "68951171",
"date_amm": "1985-06-19",
"type_amm": "Procédure nationale",
"numero_ue": null,
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "poudre pour solution injectable ou pour perfusion",
"voies_administration": "intraartérielle;intracoronaire;intraveineuse;voie extracorporelle autre",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about ACTOSOLV.
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.