Veterinary Medicines

Tabic V.H. putojošā tablete vistām un tītariem

Authorised
  • Newcastle disease virus, strain V.H., Live
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Product identification

Medicine name:
Tabic V.H. putojošā tablete vistām un tītariem
Active substance:
  • Newcastle disease virus, strain V.H., Live
Target species:
  • Turkey
  • Chicken (broiler)
  • Chicken (for reproduction)
  • Chicken (layer hen)
Route of administration:
  • In drinking water use
  • Intraocular use
  • Nebulisation use

Product details

Active substance and strength:
  • Newcastle disease virus, strain V.H., Live
    1000000.00
    50% Embryo Infective Dose
    /
    1.00
    unit(s)
Pharmaceutical form:
  • Effervescent tablet
Withdrawal period by route of administration:
  • In drinking water use
    • Turkey
      • Not specified
        0
        day
    • Chicken (broiler)
      • Not specified
        0
        day
    • Chicken (for reproduction)
      • Not specified
        0
        day
    • Chicken (layer hen)
      • Not specified
        0
        day
  • Intraocular use
    • Chicken (for reproduction)
      • Not specified
        0
        day
    • Turkey
      • Not specified
        0
        day
    • Chicken (broiler)
      • Not specified
        0
        day
    • Chicken (layer hen)
      • Not specified
        0
        day
  • Nebulisation use
    • Chicken (for reproduction)
      • Not specified
        0
        day
    • Chicken (layer hen)
      • Not specified
        0
        day
    • Turkey
      • Not specified
        0
        day
    • Chicken (broiler)
      • Not specified
        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:
  • Latvia
Available 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/10/0032
Date of authorisation status change:

Documents

Combined File of all Documents

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Latvian (PDF)
Published on: 18/12/2025
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