Veterinary Medicines

Nobivac Rabies vet. 2 IE Injektionsvätska, suspension

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

Medicine name:
Nobivac Rabies vet. 2 IE Injektionsvätska, suspension
Active substance:
  • Rabies virus, strain Pasteur RIV, Inactivated
Target species:
  • Sheep
  • Goat
  • Dog
  • Horse
  • Ferret
  • Cat
  • Cattle
  • Fox
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
Withdrawal period by route of administration:
  • Intramuscular use
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI07AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Sweden
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Oriola Sweden AB
  • Intervet International B.V.
Responsible authority:
  • Swedish Medical Products Agency
Authorisation number:
  • 13376
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 18/11/2025
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 18/11/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 13/03/2025
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