SUPPLIVEN, solution à diluer pour perfusion

solution à diluer pour perfusion · intraveineuse

Directory source checks passedOriginal source language: French

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

Formsolution à diluer pour perfusion

Routeintraveineuse

Ingredient entries9

CountryFrance

Product identity

At a glance

Authorisation holder: FRESENIUS KABI FRANCE
Authorisation status: Autorisation active
Market status: Commercialisée
Country: France
Source reference: CIS 60307630

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 SUPPLIVEN, solution à diluer pour perfusion
Ingredient	Strength / reference	Source role
IODURE DE POTASSIUMsolution	166 microgrammesune ampoule de 10 mL	SAGroup 9
CHLORURE DE ZINCsolution	10,5 mgune ampoule de 10 mL	SAGroup 4
MOLYBDATE DE SODIUM DIHYDRATÉsolution	48,5 microgrammesune ampoule de 10 mL	SAGroup 1
FLUORURE DE SODIUMsolution	2,1 mgune ampoule de 10 mL	SAGroup 8
CHLORURE DE CHROME HEXAHYDRATÉsolution	53,3 microgrammesune ampoule de 10 mL	SAGroup 7
CHLORURE DE MANGANÈSE TÉTRAHYDRATÉsolution	198 microgrammesune ampoule de 10 mL	SAGroup 5
SÉLÉNITE DE SODIUMsolution	173 microgrammesune ampoule de 10 mL	SAGroup 2
CHLORURE DE CUIVRE DIHYDRATÉsolution	1,02 mgune ampoule de 10 mL	SAGroup 6
CHLORURE FERRIQUE HEXAHYDRATÉsolution	5,4 mgune ampoule de 10 mL	SAGroup 3

Pack references

Presentations (1)

20 ampoule(s) polypropylène de 10 ml

CIP13 3400930013748

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 60307630 · 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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