France · Source-listed medicine information
France / CIS 65210377
VONCENTO 1000 UI FVIII/2400 UI FVW (10 ml de solvant), poudre et solvant pour solution injectable/perfusion
poudre et solvant pour solution injectable ou pour perfusion · intraveineuse
Source data retrieved: 2026-09-17. Clinical review is not yet available.
Product identity
At a glance
- Authorisation holder
- CSL BEHRING (ALLEMAGNE)
- Authorisation status
- Autorisation active
- Market status
- Commercialisée
- Country
- France
- Source reference
- CIS 65210377
Reported market status does not confirm current pharmacy stock.
From the official composition record
Ingredients & strength
Source entries are shown individually. An active substance (SA) and its reference moiety (FT) may describe the same ingredient; do not add their strengths together.
| Ingredient | Strength / reference | Source role |
|---|---|---|
| FACTEUR VIII DE COAGULATION HUMAIN poudre | 1000 UI10 ml | SAGroup 1 |
| FACTEUR WILLEBRAND DE COAGULATION HUMAINpoudre | 2400 UI10 ml | SAGroup 2 |
Pack references
Presentations (1)
CIP13 3400958563904
Présentation active · Déclaration de commercialisationFrom the French medicines authority
Official documents
The official product entry provides access to the patient leaflet and professional product information when available. Documents are in French and availability varies by medicine.
Open the official product entryBDPM · CIS 65210377 · Opens in a new tabCheck the medicine name, strength and form against your pack. The authority’s current documents may be newer than the catalogue snapshot shown here.
Where this information comes from
Sources & dates
Base de données publique des médicaments (BDPM), France. Retrieval dates record when we obtained the source files; they are not clinical review dates or a guarantee of current stock.
| Source file | Retrieved | Source file modified |
|---|---|---|
| fr_products.txt | Not supplied | |
| fr_composition.txt | Not supplied | |
| fr_packs.txt | Not supplied |
Directory source checks cover the factual catalogue record.Molindra clinical guidance has not yet been reviewed or published for this medicine.
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