AQUAVAC VIBRIO ORAL
AQUAVAC VIBRIO ORAL
Authorised
- Vibrio anguillarum, serotype O1, strain 78-SKID, Inactivated
- Vibrio ordalii, strain MSC275, Inactivated
Product identification
Medicine name:
AQUAVAC VIBRIO ORAL
AQUAVAC VIBRIO
Active substance:
- Vibrio anguillarum, serotype O1, strain 78-SKID, Inactivated
- Vibrio ordalii, strain MSC275, Inactivated
Target species:
-
Trout
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Vibrio anguillarum, serotype O1, strain 78-SKID, Inactivated60.00/Relative Percentage Survival1.00Dose
-
Vibrio ordalii, strain MSC275, Inactivated60.00/Relative Percentage Survival1.00Dose
Pharmaceutical form:
-
Oral emulsion
Withdrawal period by route of administration:
-
Oral use
- Trout
-
All relevant tissuesno withdrawal periodWithdrawal period is 0 days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI10BB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Package description:
- 1000 ml bottle (10 000 doses as revaccination scheme, 5000 doses as primary vaccination)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet Hellas A.E.
Marketing authorisation date:
Manufacturing sites for batch release:
- Merck Sharp & Dohme Animal Health S.L.
- MSD Animal Health UK Limited
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 16217/13-03-2008/K-0163701
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0165/001
Concerned member states:
-
Cyprus
-
Greece
-
Italy
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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