Veterinary Medicines

AviPro SALMONELLA VAC E Lyophilisate for suspension for chickens

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

Medicine name:
AviPro SALMONELLA VAC E Lyophilisate for suspension for chickens
AVIPRO SALMONELLA VAC E
Active substance:
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live
Target species:
  • Chicken
  • Chicken (chick)
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain Sm24/Rif12/Ssq, Live
    600000000.00
    Colony forming unit
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for suspension
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken
      • Egg
        0
        day
      • Meat and offal
        21
        day
    • Chicken (chick)
      • Egg
        0
        day
      • 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:
  • Slovenia
Package description:
  • (ID6): 1 Box with 10 Vials (Glass) with 5000 vaccine doses (50000 vaccine doses)
  • (ID5): 1 Box with 1 Vial (Glass) with 5000 vaccine doses (5000 vaccine doses)
  • (ID4): 1 Box with 10 Vials (Glass) with 2000 vaccine doses (20000 vaccine doses)
  • (ID3): 1 Box with 1 Vial (Glass) with 2000 vaccine doses (2000 vaccine doses)
  • (ID2): 1 Box with 10 Vials (Glass) with 1000 vaccine doses (10000 vaccine doses)
  • (ID1): 1 Box with 1 Vial (Glass) with 1000 vaccine doses (1000 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:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0026/001
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

English (PDF)
Published on: 3/03/2022
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Slovenian (PDF)
Published on: 3/03/2022
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 3/03/2022
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