Veterinary Medicines

Nobivac Rabies Suspensie voor injectie

Authorised
  • Rabies virus, strain Pasteur RIV, Inactivated
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Product identification

Medicine name:
Nobivac Rabies Suspensie voor injectie
Nobivac Rabies Suspension injectable
Nobivac Rabies Injektionssuspension
Active substance:
  • Rabies virus, strain Pasteur RIV, Inactivated
Target species:
  • Sheep
  • Dog
  • Cat
  • Cattle
  • Horse
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Rabies virus, strain Pasteur RIV, Inactivated
    2.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Sheep
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Dog
    • Cat
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
  • Subcutaneous use
    • Cat
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI07AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Nobivac Rabies 50 Vials with 1 dose of Suspension for injection
  • Nobivac Rabies 25 Vials with 1 dose of Suspension for injection
  • Nobivac Rabies 10 Vials with 1 dose of Suspension for injection
  • Nobivac Rabies 1 Vial with 1 dose of 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:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V138686
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
Download
French (PDF)
Published on: 22/03/2022
Download
German (PDF)
Published on: 22/03/2022
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