Veterinary Medicine Information website

FIXR HP ERY emulsion for injection for pigs

Authorised
  • Haemophilus parasuis, serotype 13, Inactivated
  • Haemophilus parasuis, serotype 5, Inactivated
  • Haemophilus parasuis, serotype 1, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
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Product identification

Medicine name:
FIXR HP ERY emulsion for injection for pigs
Active substance:
  • Haemophilus parasuis, serotype 13, Inactivated
  • Haemophilus parasuis, serotype 5, Inactivated
  • Haemophilus parasuis, serotype 1, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Haemophilus parasuis, serotype 13, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
  • Haemophilus parasuis, serotype 5, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
  • Haemophilus parasuis, serotype 1, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
  • Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
  • Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
    1.00
    unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • 60 ml vial plastic vials (HDPE) containing 50 ml of the vaccine. Vials are hermetically sealed with puncturable chlorobutyl rubber stoppers, fitted with aluminium caps or flip off caps and placed in paper cardboard.
  • 120 ml vial plastic vials (HDPE) containing 100 ml of the vaccine. Vials are hermetically sealed with puncturable chlorobutyl rubber stoppers, fitted with aluminium caps or flip off caps and placed in paper cardboard.

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:
  • Kernfarm B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 124851
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0328/001
Concerned member states:
  • Belgium
  • Germany

Documents

Combined File of all Documents

English (PDF)
Published on: 6/01/2026
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Dutch (PDF)
Published on: 6/01/2026
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