Veterinary Medicines

Nobivac Rabies Zawiesina do wstrzykiwań

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

Medicine name:
Nobivac Rabies Zawiesina do wstrzykiwań
Active substance:
  • Rabies virus, strain Pasteur RIV, Inactivated
Target species:
  • Cattle
  • Sheep
  • Goat
  • Horse
  • Cat
  • Ferret
  • Fox
  • Dog
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Rabies virus, strain Pasteur RIV, Inactivated
    2.00
    international unit(s)
    /
    1.00
    international unit(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Ferret
      • All relevant tissues
        no withdrawal period
    • Fox
      • All relevant tissues
        no withdrawal period
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Ferret
      • All relevant tissues
        no withdrawal period
    • Fox
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI07AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:

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:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 0472
Date of authorisation status change:

Documents

Labelling

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Polish (PDF)
Published on: 18/08/2025
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Package Leaflet

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Polish (PDF)
Published on: 18/08/2025
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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.
Polish (PDF)
Published on: 18/08/2025
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