MULTIBIC 2 mmol/l POTASSIUM, solution pour hémodialyse/hémofiltration

solution et solution pour hémodialyse pour hémofiltration · hémodialyse / hémofiltration / voie extracorporelle autre

Directory source checks passedOriginal source language: French

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

Formsolution et solution pour hémodialyse pour hémofiltration

Routehémodialyse / hémofiltration / voie extracorporelle autre

Ingredient entries7

CountryFrance

Product identity

At a glance

Authorisation holder: FRESENIUS MEDICAL CARE DEUTSCHLAND (ALLEMAGNE)
Authorisation status: Autorisation active
Market status: Commercialisée
Country: France
Source reference: CIS 63515348

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 MULTIBIC 2 mmol/l POTASSIUM, solution pour hémodialyse/hémofiltration
Ingredient	Strength / reference	Source role
BICARBONATE DE SODIUMgrand compartiment	3,104 g1000 ml	SAGroup 8
CHLORURE DE SODIUMgrand compartiment	6,453 g1000 ml	SAGroup 7
CHLORURE DE POTASSIUMpetit compartiment	2,982 g1000 ml	SAGroup 6
CALCIUM (CHLORURE DE) DIHYDRATÉpetit compartiment	4,410 g1000 ml	SAGroup 3
GLUCOSE ANHYDREpetit compartiment	20 g1000 ml	FTGroup 5
CHLORURE DE MAGNÉSIUM HEXAHYDRATÉpetit compartiment	2,033 g1000 ml	SAGroup 4
GLUCOSE MONOHYDRATÉpetit compartiment	22 g1000 ml	SAGroup 5

Pack references

Presentations (1)

2 poches bicompartimentées - petit compartiment polytéréphtalate polyamide polyoléfine de 250 ml - grand compartiment polytéréphtalate polyamide polyoléfine de 4750 ml équipées d’un connecteur HF, d’un connecteur luer-lock et d’un port d’injection

CIP13 3400934694479

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 63515348 · 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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