Veterinary Medicines

PESTIHOLVAC FORTE

Authorised
  • Newcastle disease virus, strain La Sota, Inactivated
  • Pasteurella multocida, strain Ar, Inactivated
  • Pasteurella multocida, strain Mh, Inactivated
  • Pasteurella multocida, strain Or, Inactivated
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Product identification

Medicine name:
PESTIHOLVAC FORTE
Active substance:
  • Newcastle disease virus, strain La Sota, Inactivated
  • Pasteurella multocida, strain Ar, Inactivated
  • Pasteurella multocida, strain Mh, Inactivated
  • Pasteurella multocida, strain Or, Inactivated
Target species:
  • Pheasant
  • Guinea fowl
  • Chicken
  • Turkey
Route of administration:
  • Transplacental use

Product details

Active substance and strength:
  • Newcastle disease virus, strain La Sota, Inactivated
    4.00
    log2 haemagglutination inhibiting unit(s)
    /
    0.30
    millilitre(s)
  • Pasteurella multocida, strain Ar, Inactivated
    70.00
    Percentage protective dose
    /
    0.30
    millilitre(s)
  • Pasteurella multocida, strain Mh, Inactivated
    70.00
    Percentage protective dose
    /
    0.30
    millilitre(s)
  • Pasteurella multocida, strain Or, Inactivated
    70.00
    Percentage protective dose
    /
    0.30
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Transplacental use
    • Pheasant
      • Meat and offal
        0
        day
      • Eggs
        0
        day
    • Guinea fowl
      • Meat and offal
        0
        day
      • Eggs
        0
        day
    • Chicken
      • Meat and offal
        0
        day
      • Eggs
        0
        day
    • Turkey
      • Meat and offal
        0
        day
      • Eggs
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AL04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised 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:
  • Romvac Company S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Romvac Company S.A.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 110088
Date of authorisation status change:

Documents

Combined File of all Documents

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Romanian (PDF)
Published on: 16/04/2025
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