FIXR HP ERY emulsion for injection for pigs
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
Product identification
Medicine name:
FIXR HP ERY emulsion for injection for pigs
FIXR HP Ery Emulsie voor injectie
FIXR HP Ery Emulsion injectable
FIXR HP Ery Emulsion zur Injektion
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, Inactivated1.00/unit(s)1.00millilitre(s)
-
Haemophilus parasuis, serotype 5, Inactivated1.00/unit(s)1.00millilitre(s)
-
Haemophilus parasuis, serotype 1, Inactivated1.00/unit(s)1.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated1.00/unit(s)1.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated1.00/unit(s)1.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated1.00/unit(s)1.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated1.00/unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offalno withdrawal period0 days
-
Meat and offalno withdrawal period0 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- 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.
- 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.
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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V555902
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0328/001
Concerned member states:
-
Belgium
-
Germany
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Combined File of all Documents
English (PDF)
Download Published on: 22/01/2025
Labelling
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