ZEFYLTI 48 MU/0,5 mL, solution injectable/pour perfusion en seringue préremplie

solution injectable ou pour perfusion · intraveineuse / sous-cutanée

Directory source checks passedOriginal source language: French

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

Formsolution injectable ou pour perfusion

Routeintraveineuse / sous-cutanée

Ingredient entries1

CountryFrance

Product identity

At a glance

Authorisation holder: CURATEQ BIOLOGICS (MALTE)
Authorisation status: Autorisation active
Market status: Commercialisée
Country: France
Source reference: CIS 60612685

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 ZEFYLTI 48 MU/0,5 mL, solution injectable/pour perfusion en seringue préremplie
Ingredient	Strength / reference	Source role
FILGRASTIM solution	480 microgrammes (48 MU)une seringue préremplie de 0,5 mL	SAGroup 1

Pack references

Presentations (2)

1 seringue(s) préremplie(s) en verre de 0,5 ml avec protège-aiguille

CIP13 3400930321126

Présentation active · Déclaration de commercialisation

5 seringue(s) préremplie(s) en verre de 0,5 ml avec protège-aiguille

CIP13 3400930321133

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 60612685 · 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 file	Retrieved	Source file modified
fr_products.txt	2026-09-17	Not supplied
fr_composition.txt	2026-09-17	Not supplied
fr_packs.txt	2026-09-17	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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