Veterinary Medicines

POULVAC TRT VACCINE, LYOPHILISATE FOR SUSPENSION FOR SPRAY, EYE DROP OR NOSE DROP ADMINISTRATION FOR TURKEYS

Authorised
  • Turkey rhinotracheitis virus, strain Clone K, Live
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Product identification

Medicine name:
POULVAC TRT VACCINE, LYOPHILISATE FOR SUSPENSION FOR SPRAY, EYE DROP OR NOSE DROP ADMINISTRATION FOR TURKEYS
Poulvac TRT
Active substance:
  • Turkey rhinotracheitis virus, strain Clone K, Live
Target species:
  • Turkey
Route of administration:
  • Ocular use
  • Intranasal use
  • Oculonasal use

Product details

Active substance and strength:
  • Turkey rhinotracheitis virus, strain Clone K, Live
    1584.89
    cell culture infective dose 50
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for suspension
Withdrawal period by route of administration:
  • Ocular use
    • Turkey
      • All relevant tissues
        0
        day
  • Intranasal use
    • Turkey
      • All relevant tissues
        0
        day
  • Oculonasal use
    • Turkey
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01CD01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Package description:
  • Cardboard boxes containing 1 vial of 1,000 doses
  • Cardboard boxes containing 1 vial of 2,000 doses
  • Cardboard boxes containing 1 vial of 5,000 doses
  • Cardboard boxes containing 10 vials of 1,000 doses
  • Cardboard boxes containing 10 vials of 2,000 doses
  • Cardboard boxes containing 10 vials of 5,000 doses

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Zoetis Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
  • Paul-Ehrlich-Institut
Authorisation number:
  • PEI.V.01721.01.1
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0412/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • Germany
  • Greece
  • Italy
  • Netherlands
  • Portugal
  • 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.
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
Download
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