Veterinary Medicines

AviPro® SALMONELLA VAC T Lyophilisate for use in drinking water

Authorised
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain Nal2/Rif9/Rtt, Live
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Product identification

Medicine name:
AviPro® SALMONELLA VAC T Lyophilisate for use in drinking water
AviPro Salmonella vac T, Lyofilizát pro podání v pitné vodě
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
    600000000.00
    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:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:
  • (ID1): 1 Box with 1 Vial (Glass) with 500 vaccine doses (500 vaccine doses)
  • (ID10): 1 Box with 1 Vial (Glass) with 2000 vaccine doses (2000 vaccine doses)
  • (ID12): 1 Box with 10 Vials (Glass) with 2000 vaccine doses (20000 vaccine doses)
  • (ID13): 1 Box with 1 Vial (Glass) with 2500 vaccine doses (2500 vaccine doses)
  • (ID15): 1 Box with 10 Vials (Glass) with 2500 vaccine doses (25000 vaccine doses)
  • (ID3): 1 Box with 10 Vials (Glass) with 500 vaccine doses (5000 vaccine doses)
  • (ID4): 1 Box with 1 Vial (Glass) with 1000 vaccine doses (1000 vaccine doses)
  • (ID6): 1 Box with 10 Vials (Glass) with 1000 vaccine doses (10000 vaccine doses)
  • (ID7): 1 Box with 1 Vials (Glass) with 1500 vaccine doses (1500 vaccine doses)
  • (ID9): 1 Box with 10 Vials (Glass) with 1500 vaccine doses (15000 vaccine doses)

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:
  • Lohmann Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lohmann Animal Health GmbH
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/002/06-C
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0226/001
Concerned member states:
  • Belgium
  • Czechia
  • Greece
  • Italy
  • Netherlands
  • Portugal
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 2/02/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 2/02/2024
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 2/02/2024
Download

Combined File of all Documents

English (PDF)
Published on: 30/01/2024
Download
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