Veterinary Medicines

AviPro® SALMONELLA VAC T Lyophilisate for use in drinking water

Authorised
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, Live
Download as PDF

Product identification

Medicine name:
AviPro® SALMONELLA VAC T Lyophilisate for use in drinking water
Avipro Salmonella VAC T liofilizado para uso na água de bebida
Active substance:
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, Live
Target species:
  • Chicken
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, 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
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
Available in:
  • Portugal
Package description:
  • (ID9) 15000 Dose: Box (Cardboard) with 10 Vial (Glass) each with 1500 Dose
  • (ID7) 1500 Dose: Box (Cardboard) with 1 Vial (Glass) with 1500 Dose
  • (ID6) 10000 Dose: Box (Cardboard) with 10 Vial (Glass) each with 1000 Dose
  • (ID4) 1000 Dose: Box (Cardboard) with 1 Vial (Glass) with 1000 Dose
  • (ID3) 5000 Dose: Box (Cardboard) with 10 Vial (Glass) each with 500 Dose
  • (ID15) 25000 Dose: Box (Cardboard) with 10 Vial (Glass) each with 2500 Dose
  • (ID13) 2500 Dose: Box (Cardboard) with 1 Vial (Glass) with 2500 Dose
  • (ID12) 20000 Dose: Box (Cardboard) with 10 Vial (Glass) each with 2000 Dose
  • (ID10) 2000 Dose: Box (Cardboard) with 1 Vial (Glass) with 2000 Dose
  • (ID1) 500 Dose: Box (Cardboard) with 1 Vial (Glass) with 500 Dose

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lohmann Animal Health GmbH
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • R763/06 DGV
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0226/001
Concerned member states:
  • Austria
  • Belgium
  • Cyprus
  • Czechia
  • France
  • Greece
  • Hungary
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 30/01/2024
Download
Portuguese (PDF)
Published on: 19/01/2023
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."