Veterinary Medicines Information website

Rabitec (--) - Oral suspension

Authorised
  • Rabies virus, strain SPBN GASGAS, Live
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Product identification

Medicine name:
Rabitec (--) - Oral suspension
Active substance:
  • Rabies virus, strain SPBN GASGAS, Live
Target species:
  • Fox
  • Raccoon dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Rabies virus, strain SPBN GASGAS, Live
    Presentation_strength:10 ⁶·⁸ to 10⁸·¹ FFU Reference:Hse Index:0
Pharmaceutical form:
  • Oral suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI07BD
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)
Package description:
  • Packaging:40 × 20 baits; suspension: blister (PVC-Alu); bait: matrix, Package_size:800 bait, Content:Suspension: 1.7 ml (one dose); bait: PE bag
  • Packaging:800 baits; suspension: blister (PVC-Alu); bait: matrix, Package_size:800 bait, Content:Suspension: 1.7 ml (one dose); bait: PE sleeve
  • Packaging:4 × 200 baits; suspension: blister (PVC-Alu); bait: matrix, Package_size:800 bait, Content:Suspension: 1.7 ml (one dose); bait: PE bag

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Tiergesundheit (Riems) GmbH
Responsible authority:
  • European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change: