France · Source-listed medicine information
France / CIS 67619892
REPEVAX, suspension injectable en seringue préremplie. Vaccin diphtérique, tétanique, coquelucheux (acellulaire, multicomposé) et poliomyélitique (inactivé), (adsorbé, à teneur réduite en antigène(s))
suspension injectable · intramusculaire
Source data retrieved: 2026-09-17. Clinical review is not yet available.
Product identity
At a glance
- Authorisation holder
- SANOFI WINTHROP INDUSTRIE
- Authorisation status
- Autorisation active
- Market status
- Commercialisée
- Country
- France
- Source reference
- CIS 67619892
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 |
|---|---|---|
| ANATOXINE DIPHTÉRIQUE suspension | supérieur ou égal à 2 UIune dose de 0,5 ml | SAGroup 2 |
| ANATOXINE TÉTANIQUE suspension | supérieur ou égal à 20 UIune dose de 0,5 ml | SAGroup 1 |
| VIRUS POLIOMYÉLITIQUE SOUCHE MEF-1 DE TYPE 2 INACTIVÉ suspension | 7 UDune dose de 0,5 ml | SAGroup 8 |
| VIRUS POLIOMYÉLITIQUE SOUCHE SAUKETT DE TYPE 3 INACTIVÉ suspension | 26 UDune dose de 0,5 ml | SAGroup 9 |
| VIRUS POLIOMYELITIQUE SOUCHE MAHONEY DE TYPE 1 INACTIVÉ suspension | 29 UDune dose de 0,5 ml | SAGroup 7 |
| ANTIGÈNE PERTUSSIQUE : PERTACTINE suspension | 3 microgrammesune dose de 0,5 ml | SAGroup 6 |
| ANTIGÈNES PERTUSSIQUES : FIMBRIAE TYPE 2 ET 3 suspension | 5 microgrammesune dose de 0,5 ml | SAGroup 5 |
| ANTIGÈNE PERTUSSIQUE : HÉMAGGLUTININE FILAMENTEUSE suspension | 5 microgrammesune dose de 0,5 ml | SAGroup 4 |
| ANTIGÈNE PERTUSSIQUE : ANATOXINE PERTUSSIQUE suspension | 2,5 microgrammesune dose de 0,5 ml | SAGroup 3 |
Pack references
Presentations (2)
CIP13 3400936873742
Présentation active · Déclaration de commercialisationCIP13 3400936873971
Présentation active · Déclaration d'arrêt 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 67619892 · 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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