Veterinary Medicines

Nobilis Salenvac T suspension for injection for chickens

Authorised
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain DT104, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT4, Inactivated
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Product identification

Medicine name:
Nobilis Salenvac T suspension for injection for chickens
Nobilis Salenvac T
Active substance:
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain DT104, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT4, Inactivated
Target species:
  • Chicken
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain DT104, Inactivated
    1.00
    relative potency
    /
    0.50
    millilitre(s)
  • Salmonella enterica, subsp. enterica, serovar Enteritidis, strain PT4, Inactivated
    1.00
    relative potency
    /
    0.50
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Chicken
      • Meat and offal
        0
        day
      • Egg
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AB01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:
  • Cardboard box containing a 500 ml (1000 doses) low density polyethylene multi-dose bottle closed with an aluminium ring on top of a rubber stopper
  • Cardboard box containing a 250 ml (500 doses) low density polyethylene multi-dose bottle closed with an aluminium ring on top of a rubber stopper

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Paul-Ehrlich-Institut
Authorisation number:
  • PEI.V.02970.01.1
Date of authorisation status change:
Reference member state:
  • Italy
Procedure number:
  • IT/V/0137/001
Concerned member states:
  • Austria
  • Czechia
  • Denmark
  • France
  • Germany
  • Greece
  • Hungary
  • Lithuania
  • Luxembourg
  • Netherlands
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 6/10/2025
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Italian (PDF)
Published on: 16/02/2022
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 23/06/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 23/06/2023
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