Veterinary Medicine Information website

NEMOVAC liofilizat pentru suspensie pentru administrare oculonazală/ în apa de băut pentru găini

Authorised
  • Turkey rhinotracheitis virus, strain PL21, Live
Download as PDF

Product identification

Medicine name:
NEMOVAC liofilizat pentru suspensie pentru administrare oculonazală/ în apa de băut pentru găini
Active substance:
  • Turkey rhinotracheitis virus, strain PL21, Live
Target species:
  • Chicken (broiler)
  • Chicken (for reproduction)
  • Chicken (pullet for egg production, future layer)
Route of administration:
  • Oral use
  • Nebulisation use

Product details

Active substance and strength:
  • Turkey rhinotracheitis virus, strain PL21, Live
    2.30
    log10 50% cell culture infectious dose
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Lyophilisate for oculonasal suspension/use in drinking water
Withdrawal period by route of administration:
  • Oral use
    • Chicken (broiler)
      • Meat and offal
        0
        day
    • Chicken (for reproduction)
      • Meat and offal
        0
        day
    • Chicken (pullet for egg production, future layer)
      • Meat and offal
        0
        day
      • Eggs
        0
        day
  • Nebulisation use
    • Chicken (broiler)
      • Meat and offal
        0
        day
    • Chicken (pullet for egg production, future layer)
      • Meat and offal
        0
        day
      • Eggs
        0
        day
    • Chicken (for reproduction)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD01
Legal status of supply:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Romania
Available in:
  • Romania
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 120092
Date of authorisation status change:

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 24/12/2025
Download