Veterinary Medicines

FIXR RHINI suspension for injection for pigs

Authorised
  • Pasteurella multocida, toxoid
  • Pasteurella multocida, serogroup A, Inactivated
  • Bordetella bronchiseptica, strain F236, Inactivated
  • Pasteurella multocida, serogroup D, Inactivated
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Product identification

Medicine name:
FIXR RHINI suspension for injection for pigs
FIXR RHINI suspension injectable pour porcins
FIXR RHINI suspensie voor injectie voor varkens
FIXR RHINI Injektionssuspension für Schweine
Active substance:
  • Pasteurella multocida, toxoid
  • Pasteurella multocida, serogroup A, Inactivated
  • Bordetella bronchiseptica, strain F236, Inactivated
  • Pasteurella multocida, serogroup D, Inactivated
Target species:
  • Pig
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Pasteurella multocida, toxoid
    2.00
    microgram(s)
    /
    1.00
    Dose
  • Pasteurella multocida, serogroup A, Inactivated
    80.00
    percentage protection
    /
    1.00
    Dose
  • Bordetella bronchiseptica, strain F236, Inactivated
    32.00
    titre
    /
    1.00
    Dose
  • Pasteurella multocida, serogroup D, Inactivated
    80.00
    percentage protection
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Pig
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • 20 ml injection vial of hydrolytic class I glass closed with a rubber stopper and an aluminium seal in a cardboard box
  • 20 ml injection vial of hydrolytic class I glass closed with a rubber stopper and an aluminium seal in a polystyrene case
  • 100 ml injection vial of hydrolytic class I glass closed with a rubber stopper and an aluminium seal in a cardboard box
  • 100 ml injection vial of hydrolytic class I glass closed with a rubber stopper and an aluminium seal in a polystyrene case
  • 20 ml polypropylene bottle closed with a rubber stopper and an aluminium seal in a cardboard box
  • 20 ml polypropylene bottle closed with a rubber stopper and an aluminium seal in a polystyrene case
  • 100 ml polypropylene bottle closed with a rubber stopper and an aluminium seal in a cardboard box
  • 100 ml polypropylene bottle closed with a rubber stopper and an aluminium seal in a polystyrene case

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 19(1) of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Kernfarm B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0393/001
Concerned member states:
  • Belgium

Documents

Combined File of all Documents

English (PDF)
Published on: 14/01/2025
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