Veterinary Medicines

Rhiniffa T Suspensie voor injectie

Not authorised
  • Bordetella bronchiseptica, Inactivated
  • Pasteurella multocida, toxoid
  • Pasteurella multocida, Serotype D, Inactivated
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Product identification

Medicine name:
Rhiniffa T Suspensie voor injectie
Rhiniffa T Suspension injectable
Rhiniffa T Injektionssuspension
Active substance:
  • Bordetella bronchiseptica, Inactivated
  • Pasteurella multocida, toxoid
  • Pasteurella multocida, Serotype D, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Bordetella bronchiseptica, Inactivated
    0.90
    log10 serum neutralising unit(s)
    /
    2.00
    millilitre(s)
  • Pasteurella multocida, toxoid
  • Pasteurella multocida, Serotype D, Inactivated
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Belgium
Package description:
  • Rhiniffa T 1 x 50 ml Vial Suspension for injection
  • Rhiniffa T 1 x 200 ml Vial Suspension for injection
  • Rhiniffa T 1 x 20 ml Vial Suspension for injection
  • Rhiniffa T 1 x 10 ml Vial Suspension for injection
  • Rhiniffa T 5 x 2 ml Vial Suspension for injection
  • Rhiniffa T 10 x 2 ml Vial Suspension for injection

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:
  • Boehringer Ingelheim Animal Health Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V156441
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.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
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French (PDF)
Published on: 22/03/2022
Download
German (PDF)
Published on: 22/03/2022
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