Veterinary Medicine Information website

Nobivac Rabies, süstesuspensioon koertele, kassidele, veistele, lammastele, kitsedele, rebastele, tuhkrutele ja hobustele

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

Medicine name:
Nobivac Rabies, süstesuspensioon koertele, kassidele, veistele, lammastele, kitsedele, rebastele, tuhkrutele ja hobustele
Active substance:
  • Rabies virus, strain Pasteur RIV, Inactivated
Target species:
  • Dog
  • Cat
  • Cattle
  • Sheep
  • Goat
  • Fox
  • Ferret
  • Horse
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
    dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        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:
  • Estonia
Available in:
  • Estonia
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:
  • State Agency Of Medicines
Authorisation number:
  • 1150
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.
Estonian (PDF)
Published on: 21/01/2026
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