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Veterinary Medicines

AviPro SALMONELLA VAC E Lyophilisate for suspension for chickens

Authorised
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live

Product identification

Medicine name:
AviPro SALMONELLA VAC E Lyophilisate for suspension for chickens
Avipro Salmonella Vac E Lyofilisaat voor suspensie
Avipro Salmonella Vac E Lyophilisat pour suspension
Avipro Salmonella Vac E Lyophilisat zur Herstellung einer Suspension
Active substance:
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live
Target species:
  • Chicken
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live
    100000000.00
    Colony forming unit
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken
      • Meat and offal
        21
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AE01
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • (ID6) 50000 Dose: Box (cardboard) with 10 Vial (Glass type I) each with 5000 Dose, closed with Stopper (rubber) and Kappe (aluminium)
  • (ID5) 5000 Dose: Box (cardboard) with 1 Vial (Glass type I) with 5000 Dose, closed with Kappe (aluminium) and Stopper (rubber)
  • (ID4) 20000 Dose: Box (cardboard) with 10 Vial (Glass type I) each with 2000 Dose, closed with Stopper (rubber) and Kappe (aluminium)
  • (ID3) 2000 Dose: Box (cardboard) with 1 Vial (Glass type I) with 2000 Dose, closed with Stopper (rubber) and Kappe (aluminium)
  • (ID2) 10000 Dose: Box (cardboard) with 10 Vial (Glass type I) each with 1000 Dose, closed with Stopper (rubber) and Kappe (aluminium)
  • (ID1) 1000 Dose: Box (cardboard) with 1 Vial (Glass type I) with 1000 Dose, closed with Stopper (rubber) and Kappe (aluminium)

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lohmann Animal Health GmbH
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V232985
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0215/001
Concerned member states:
  • Austria
  • Belgium
  • Estonia
  • France
  • Greece
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Portugal
  • Slovenia
  • Spain

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 17/10/2025
French (PDF)
Published on: 17/10/2025
German (PDF)
Published on: 17/10/2025

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 17/10/2025
French (PDF)
Published on: 17/10/2025
German (PDF)
Published on: 17/10/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 17/10/2025
French (PDF)
Published on: 17/10/2025
German (PDF)
Published on: 17/10/2025

Combined File of all Documents

English (PDF)
Published on: 13/02/2026
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