Veterinary Medicines

BioEquin FT suspensija injekcijām zirgiem

Authorised
  • Clostridium tetani, toxoid
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/08, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Morava/95, Inactivated
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Product identification

Medicine name:
BioEquin FT suspensija injekcijām zirgiem
Active substance:
  • Clostridium tetani, toxoid
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/08, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Morava/95, Inactivated
Target species:
  • Horse
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Clostridium tetani, toxoid
    30.00
    international unit(s)
    /
    1.00
    unit(s)
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/08, Inactivated
    Viena deva (1 ml) satur: ≥ 5 log2 HIT (specifisko antivielu vidējais ģeometriskais titrs jūrascūciņu asins serumā, noteikts ar hemaglutinācijas inhibīcijas testu)
  • Influenza A virus, subtype H3N8, strain A/equine/Morava/95, Inactivated
    Viena deva (1 ml) satur: ≥ 5 log2 HIT (specifisko antivielu vidējais ģeometriskais titrs jūrascūciņu asins serumā, noteikts ar hemaglutinācijas inhibīcijas testu)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI05AL01
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:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/20/0021
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Latvian (PDF)
Published on: 11/12/2024
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Package Leaflet

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Latvian (PDF)
Published on: 11/12/2024
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Labelling

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Latvian (PDF)
Published on: 11/12/2024
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