France · Source-listed medicine information

France / CIS 65570603

PRADAXA 110 mg, gélule

gélule · orale

Directory source checks passedOriginal source language: French

Source data retrieved: 2026-09-17. Clinical review is not yet available.

Formgélule
Routeorale
Ingredient entries2
CountryFrance

Product identity

At a glance

Authorisation holder
BOEHRINGER INGELHEIM INTERNATIONAL
Authorisation status
Autorisation active
Market status
Commercialisée
Country
France
Source reference
CIS 65570603

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.

Source composition entries for PRADAXA 110 mg, gélule
IngredientStrength / referenceSource role
DABIGATRAN ÉTEXILATE BASEgélule110 mgune géluleFTGroup 1
DABIGATRAN ÉTEXILATE (MÉSILATE DE)gélule126,83 mgune géluleSAGroup 1

Pack references

Presentations (3)

10 plaquette(s) thermoformée(s) aluminium copolymères chlorure de vinyle/acétate de vinyle acrylate PVC PVC-Aluminium de 1 gélule(s)

CIP13 3400938526080

Présentation active · Déclaration de commercialisation
30 plaquette(s) thermoformée(s) aluminium copolymères chlorure de vinyle/acétate de vinyle acrylate PVC PVC-Aluminium de 1 gélule(s)

CIP13 3400938526141

Présentation active · Déclaration de commercialisation
60 plaquette(s) thermoformée(s) aluminium copolymères chlorure de vinyle/acétate de vinyle acrylate PVC PVC-Aluminium de 1 gélule(s)

CIP13 3400938526202

Présentation active · Déclaration de commercialisation

From 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 65570603 · Opens in a new tab

Check 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 files and their retrieval dates
Source fileRetrievedSource file modified
fr_products.txtNot supplied
fr_composition.txtNot supplied
fr_packs.txtNot supplied

Directory source checks cover the factual catalogue record.Molindra clinical guidance has not yet been reviewed or published for this medicine.

Our sources and review process →