Veterinary Medicine Information website

Nobivac Rabies suspension for injection for dogs and cats

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

Medicine name:
Nobivac Rabies suspension for injection for dogs and cats
Active substance:
  • Rabies virus, strain Pasteur RIV, Inactivated
Target species:
  • Dog
  • Cat
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
    Dose
Pharmaceutical form:
  • Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI07AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Clear, hydrolytic glass Type I (Ph. Eur.) single dose vials with halogenobutyl rubber stopper, closed with a colour coded aluminium cap. Carton with 1 x 1 ml.
  • Clear, hydrolytic glass Type I (Ph. Eur.) single dose vials with halogenobutyl rubber stopper, closed with a colour coded aluminium cap. Carton or plastic box with 50 x 1 ml.
  • Clear, hydrolytic glass Type I (Ph. Eur.) single dose vials with halogenobutyl rubber stopper, closed with a colour coded aluminium cap.Carton or plastic box with 10 x 1ml

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 (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/170/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 24/08/2025
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