France / CIS 68664125

ZYPREXA VELOTAB 5 mg, comprimé orodispersible

comprimé orodispersible · orale

Directory source checks passedOriginal source language: French

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

Formcomprimé orodispersible
Routeorale
Ingredient entries1
CountryFrance

Product identity

At a glance

Authorisation holder
CHEPLAPHARM REGISTRATION (ALLEMAGNE)
Authorisation status
Autorisation active
Market status
Commercialisée
Country
France
Source reference
CIS 68664125

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 ZYPREXA VELOTAB 5 mg, comprimé orodispersible
IngredientStrength / referenceSource role
OLANZAPINEcomprimé5 mgun compriméSAGroup 1

Pack references

Presentations (5)

plaquette(s) thermoformée(s) aluminium de 28 comprimé(s)

CIP13 3400935454218

Présentation active · Déclaration de commercialisation
plaquette(s) thermoformée(s) aluminium de 28 comprimé(s) (distributeur parallèle : Laboratoire Mediwin Ldt)

CIP13 3400949504190

Présentation active · Déclaration de commercialisation
plaquette(s) thermoformée(s) aluminium de 28 comprimé(s) (distributeur parallèle : BB Farma)

CIP13 3400949505371

Présentation active · Déclaration de commercialisation
plaquette(s) thermoformée(s) aluminium de 28 comprimé(s) (distributeur parallèle : PHARMA LAB)

CIP13 3400949507382

Présentation active · Déclaration de commercialisation
plaquette(s) thermoformée(s) aluminium de 28 comprimé(s) (distributeur parallèle : Inter Trade Pharma)

CIP13 3400949510283

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 68664125 · 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 →