Veterinary Medicines

BioEquin F suspension for injection for horses

Authorised
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/08, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Limerick/2010, Inactivated
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Product identification

Medicine name:
BioEquin F suspension for injection for horses
BioEquin F, injekcinė suspensija arkliams
Active substance:
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/08, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Limerick/2010, Inactivated
Target species:
  • Horse
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Influenza A virus, subtype H3N8, strain A/equine/Brno/08, Inactivated
    5.00
    log2 haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
  • Influenza A virus, subtype H3N8, strain A/equine/Limerick/2010, Inactivated
    5.00
    log2 haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Milk
        0
        hour
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI05AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Lithuania
Package description:
  • glass vial 2 x 1.0 dose
  • glass vial 5 x 1.0 dose
  • glass vial 10 x 1.0 dose
  • glass vial 1 x 5.0 dose
  • glass vial 10 x 5.0 dose

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:
  • State Food And Veterinary Service
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
  • Czechia
Procedure number:
  • CZ/V/0200/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • Finland
  • France
  • Germany
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Lithuanian (PDF)
Published on: 30/07/2025
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