Rabitec (--) - Oral suspension
Rabitec (--) - Oral suspension
Authorised
- Rabies virus, strain SPBN GASGAS, Live
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, LivePresentation_strength:10 ⁶·⁸ to 10⁸·¹ FFU Reference:Hse Index:0
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Fox
-
Raccoon dog
-
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:Suspension: Blister (PVC-Alu); bait: matrix, Package_size:800 bait, Content:Suspension: 1.7 ml (one dose); bait: PE bag
- Packaging:Suspension: Blister (PVC-Alu); bait: matrix, Package_size:800 bait, Content:Suspension: 1.7 ml (one dose); bait: PE sleeve
- Packaging: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 Santé Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- IDT Biologika GmbH
- Ceva Tiergesundheit (Riems) GmbH
Responsible authority:
- European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 16/10/2024
Bulgarian (PDF)
Published on: 16/10/2024
Croatian (PDF)
Published on: 16/10/2024
Czech (PDF)
Published on: 16/10/2024
Danish (PDF)
Published on: 16/10/2024
Dutch (PDF)
Published on: 16/10/2024
Estonian (PDF)
Published on: 16/10/2024
Finnish (PDF)
Published on: 16/10/2024
French (PDF)
Published on: 16/10/2024
German (PDF)
Published on: 16/10/2024
Greek (PDF)
Published on: 16/10/2024
Hungarian (PDF)
Published on: 16/10/2024
Icelandic (PDF)
Published on: 16/10/2024
Italian (PDF)
Published on: 16/10/2024
Latvian (PDF)
Published on: 16/10/2024
Lithuanian (PDF)
Published on: 16/10/2024
Maltese (PDF)
Published on: 16/10/2024
Norwegian (PDF)
Published on: 16/10/2024
Polish (PDF)
Published on: 16/10/2024
Portuguese (PDF)
Published on: 16/10/2024
Romanian (PDF)
Published on: 16/10/2024
Slovak (PDF)
Published on: 16/10/2024
Slovenian (PDF)
Published on: 16/10/2024
Spanish (PDF)
Published on: 16/10/2024
Swedish (PDF)
Published on: 16/10/2024
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