Veterinary Medicines Information website

Equip F vet. Injektionsvätska, suspension

Authorised
  • Influenza A virus, subtype H7N7, strain A/equine/Newmarket/77, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Borlange/91, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Kentucky/1/98, Inactivated
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Product identification

Medicine name:
Equip F vet. Injektionsvätska, suspension
Active substance:
  • Influenza A virus, subtype H7N7, strain A/equine/Newmarket/77, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Borlange/91, Inactivated
  • Influenza A virus, subtype H3N8, strain A/equine/Kentucky/1/98, Inactivated
Target species:
  • Horse
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Influenza A virus, subtype H7N7, strain A/equine/Newmarket/77, Inactivated
    1.20
    log10 haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
  • Influenza A virus, subtype H3N8, strain A/equine/Borlange/91, Inactivated
    2.10
    log10 haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
  • Influenza A virus, subtype H3N8, strain A/equine/Kentucky/1/98, Inactivated
    2.40
    log10 haemagglutination inhibiting unit(s)
    /
    1.00
    Dose
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:
  • QI05AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Sweden
Available in:
  • Sweden
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Zoetis Animal Health ApS
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Swedish Medical Products Agency
Authorisation number:
  • 18954
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 26/09/2023
Updated on: 27/09/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 26/09/2023
Updated on: 27/09/2023
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 26/09/2023
Updated on: 27/09/2023
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