PANOTILE, solution pour instillation auriculaire

solution pour instillation · auriculaire

Directory source checks passedOriginal source language: French

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

Formsolution pour instillation

Routeauriculaire

Ingredient entries6

CountryFrance

Product identity

At a glance

Authorisation holder: ZAMBON FRANCE
Authorisation status: Autorisation active
Market status: Commercialisée
Country: France
Source reference: CIS 68039248

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 PANOTILE, solution pour instillation auriculaire
Ingredient	Strength / reference	Source role
SULFATE DE POLYMYXINE Bsolution	1 000 000 Ul100 ml de solution	SAGroup 1
ACÉTATE DE FLUDROCORTISONEsolution	0,1000 g100 ml de solution	SAGroup 3
SULFATE DE NÉOMYCINEsolution	1 g100 ml de solution	SAGroup 2
LIDOCAÏNEsolution	3,2457g100 ml de solution	FTGroup 4
CHLORHYDRATE DE LIDOCAÏNEsolution	4,0000 g100 ml de solution	SAGroup 4
FLUDROCORTISONEsolution	0,09 g100 ml de solution	FTGroup 3

Pack references

Presentations (1)

1 flacon(s) compte-gouttes en verre jaune(brun) de 8 ml

CIP13 3400931922537

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 68039248 · 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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