Bovilis Ringvac <9 and >21 Lyophilisate+solvent for suspension for injection
Bovilis Ringvac <9 and >21 Lyophilisate+solvent for suspension for injection
Suspended
- Trichophyton verrucosum, strain LTF-130, Live
Product identification
Medicine name:
Bovilis Ringvac <9 and >21 Lyophilisate+solvent for suspension for injection
BOVILIS RINGVAC
Active substance:
- Trichophyton verrucosum, strain LTF-130, Live
Target species:
-
Cattle
-
Cattle (calf)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Trichophyton verrucosum, strain LTF-130, Live21000000.00cells1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal0day
-
Milk0day
-
- Cattle (calf)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AP01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Suspended
Authorised in:
-
France
Package description:
- (ID2) 40 millilitre(s); 40 Dose: Box (Cardboard) with 1 Bottle (Glass) with 40 Dose and 1 Bottle (Glass) with 40 millilitre(s)
- (ID1) 10 Dose; 10 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 10 Dose and 1 Bottle (Glass) with 10 millilitre(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet
Marketing authorisation date:
This information is not available for this product.
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/0595008 3/2005
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0231/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
France
-
Greece
-
Hungary
-
Ireland
-
Luxembourg
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 14/02/2022
French (PDF)
Published on: 4/04/2022
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