ROTATEQ, solution buvable. Vaccin Rotavirus (vivant, oral)

solution buvable · orale

Directory source checks passedOriginal source language: French

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

Formsolution buvable

Routeorale

Ingredient entries5

CountryFrance

Product identity

At a glance

Authorisation holder: MERCK SHARP & DOHME (PAYS-BAS)
Authorisation status: Autorisation active
Market status: Commercialisée
Country: France
Source reference: CIS 66396810

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 ROTATEQ, solution buvable. Vaccin Rotavirus (vivant, oral)
Ingredient	Strength / reference	Source role
ROTAVIRUS RÉASSORTANT HUMAIN-BOVIN DE TYPE G1 (VIVANT) solution	au minimum 2 200 000 UIune dose de 2 ml	SAGroup 1
ROTAVIRUS RÉASSORTANT HUMAIN-BOVIN DE TYPE G2 (VIVANT) solution	au minimum 2 800 000 UIune dose de 2 ml	SAGroup 2
ROTAVIRUS RÉASSORTANT HUMAIN-BOVIN DE TYPE G3 (VIVANT) solution	au minimum 2 200 000 UIune dose de 2 ml	SAGroup 3
ROTAVIRUS RÉASSORTANT HUMAIN-BOVIN DE TYPE G4 (VIVANT) solution	au minimum 2 000 000 UIune dose de 2 ml	SAGroup 4
ROTAVIRUS RÉASSORTANT HUMAIN-BOVIN DE TYPE P1A[8] (VIVANT) solution	au minimum 2 300 000 UIune dose de 2 ml	SAGroup 5

Pack references

Presentations (1)

1 tube unidose souple polyéthylène basse densité (PEBD) suremballée(s)/surpochée(s) de 2 ml

CIP13 3400937622363

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 66396810 · 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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