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Veterinary Medicines

AviPro GUMBORO VAC Lyophilisate for suspension for chicken

Not authorised
  • Infectious bursal disease virus, strain Cu-1 M, Live

Product identification

Medicine name:
AviPro GUMBORO VAC Lyophilisate for suspension for chicken
Avipro Gumboro Vac Lyofilisaat voor gebruik in drinkwater
Avipro Gumboro Vac Lyophilisat pour administration dans l'eau de boisson
Avipro Gumboro Vac Lyophilisat zum Eingeben über das Trinkwasser
Active substance:
  • Infectious bursal disease virus, strain Cu-1 M, Live
Target species:
  • Chicken (broiler)
  • Chicken
  • Chicken (for reproduction)
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Infectious bursal disease virus, strain Cu-1 M, Live
    5011.87
    50% Embryo Infective Dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for suspension
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken (broiler)
      • Meat and offal
        0
        day
    • Chicken
      • Egg
        0
        day
      • Meat and offal
        0
        day
    • Chicken (for reproduction)
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD09
Authorisation status:
  • Surrendered
Authorised in:
  • Belgium
Package description:
  • (ID1): 1 Box with 1 Bottle (Glass) with 1000 Dose (1000 Dose)
  • (ID4): 1 Box with 10 Bottle (Glass) with 2500 Dose (25000 Dose)
  • (ID2): 1 Box with 10 Bottle (Glass) with 1000 Dose (10000 Dose)
  • (ID3): 1 Box with 1 Bottle (Glass) with 2500 Dose (2500 Dose)
  • (ID7): 1 Box with 1 Bottle (Glass) with 10000 Dose (10000 Dose)
  • (ID8): 1 Box with 10 Bottle (Glass) with 10000 Dose (100000 Dose)
  • (ID6): 1 Box with 10 Bottle (Glass) with 5000 Dose (50000 Dose)
  • (ID5): 1 Box with 1 Bottle (Glass) with 5000 Dose (5000 Dose)

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-V214952
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0206/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
Download
Dutch (PDF)
Published on: 22/03/2022
French (PDF)
Published on: 22/03/2022

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
French (PDF)
Published on: 22/03/2022
German (PDF)
Published on: 22/03/2022
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