Veterinary Medicines

V.H. + H-120 liofilizāts ūdens šķīduma pagatavošanai vistām

Authorised
  • Newcastle disease virus, strain V.H., Live
  • Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
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Product identification

Medicine name:
V.H. + H-120 liofilizāts ūdens šķīduma pagatavošanai vistām
Active substance:
  • Newcastle disease virus, strain V.H., Live
  • Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
Target species:
  • Chicken (layer hen)
  • Chicken (broiler)
  • Chicken (for reproduction)
Route of administration:
  • In drinking water use
  • Intraocular use
  • Nebulisation use

Product details

Active substance and strength:
  • Newcastle disease virus, strain V.H., Live
  • Avian infectious bronchitis virus, type Massachusetts, strain H120, Live
Pharmaceutical form:
  • Lyophilisate for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Chicken (layer hen)
      • Not specified
        0
        day
    • Chicken (broiler)
      • Not specified
        0
        day
    • Chicken (for reproduction)
      • Not specified
        0
        day
  • Intraocular use
    • Chicken (broiler)
      • Not specified
        0
        day
    • Chicken (for reproduction)
      • Not specified
        0
        day
    • Chicken (layer hen)
      • Not specified
        0
        day
  • Nebulisation use
    • Chicken (broiler)
      • Not specified
        0
        day
    • Chicken (for reproduction)
      • Not specified
        0
        day
    • Chicken (layer hen)
      • Not specified
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Package description:

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:
  • Phibro Animal Health (Poland) Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Synoptis Industrial Sp. z o.o.
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/10/0033
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.
Latvian (PDF)
Published on: 15/12/2025
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Summary of Product Characteristics

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Latvian (PDF)
Published on: 15/12/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 15/12/2025
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