Veterinary Medicines

Poulvac NDW Atenuowany wirus rzekomego pomoru ptaków (choroby Newcastle), szczep Ulster 2C nie mniej niż 10^5,7 EID50 i nie więcej niż 10^6,6 EID50. Liofilizat

Authorised
  • Newcastle disease virus, strain Ulster 2C, Live
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Product identification

Medicine name:
Poulvac NDW Atenuowany wirus rzekomego pomoru ptaków (choroby Newcastle), szczep Ulster 2C nie mniej niż 10^5,7 EID50 i nie więcej niż 10^6,6 EID50. Liofilizat
Active substance:
  • Newcastle disease virus, strain Ulster 2C, Live
Target species:
  • Turkey
  • Chicken (hen)
Route of administration:
  • Ocular use
  • In drinking water use
  • Nebulisation use
  • Nasal use

Product details

Active substance and strength:
  • Newcastle disease virus, strain Ulster 2C, Live
Pharmaceutical form:
  • Lyophilisate for solution for injection
Withdrawal period by route of administration:
  • Ocular use
    • Turkey
      • All relevant tissues
        0
        day
    • Chicken (hen)
      • All relevant tissues
        0
        day
  • In drinking water use
    • Turkey
      • All relevant tissues
        0
        day
    • Chicken (hen)
      • All relevant tissues
        0
        day
  • Nebulisation use
    • Turkey
      • All relevant tissues
        0
        day
    • Chicken (hen)
      • All relevant tissues
        0
        day
  • Nasal use
    • Turkey
      • All relevant tissues
        0
        day
    • Chicken (hen)
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
Package description:

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:
  • Zoetis Polska Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 0180
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 14/11/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 14/11/2025
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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.
Polish (PDF)
Published on: 14/11/2025
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