Veterinary Medicines

FLUEQUIN T, Injekční suspenze

Authorised
  • Influenza A virus, subtype H7N7, strain A/equine/Prague/1956, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Morava/95, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/97, Inactivated
  • Clostridium tetani, toxoid
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Product identification

Medicine name:
FLUEQUIN T, Injekční suspenze
Active substance:
  • Influenza A virus, subtype H7N7, strain A/equine/Prague/1956, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Morava/95, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/97, Inactivated
  • Clostridium tetani, toxoid
Target species:
  • Horse
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Influenza A virus, subtype H7N7, strain A/equine/Prague/1956, Inactivated
    160.00
    haemagglutinating units
    /
    1.00
    Dose
  • Influenza A virus, subtype H3N8, strain A/equine/Morava/95, Inactivated
    320.00
    haemagglutinating units
    /
    1.00
    Dose
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/97, Inactivated
    320.00
    haemagglutinating units
    /
    1.00
    Dose
  • Clostridium tetani, toxoid
    1.00
    relative potency
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI05AL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
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:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/003/04-C
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Czech (PDF)
Published on: 26/10/2022
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Package Leaflet

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Czech (PDF)
Published on: 26/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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