Fencovis, Suspension for injection
Fencovis, Suspension for injection
Authorised
- Escherichia coli, serotype O8:K35 (fimbrial adhesin F5), Inactivated
- Bovine coronavirus, Inactivated
- Bovine rotavirus, Inactivated
Product identification
Medicine name:
Fencovis Suspensie voor injectie
Fencovis Suspension injectable
Fencovis Injektionssuspension
Fencovis, Suspension for injection
Active substance:
- Escherichia coli, serotype O8:K35 (fimbrial adhesin F5), Inactivated
- Bovine coronavirus, Inactivated
- Bovine rotavirus, Inactivated
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli, serotype O8:K35 (fimbrial adhesin F5), Inactivated1.00relative potency1.00Dose
-
Bovine coronavirus, Inactivated1.00relative potency1.00Dose
-
Bovine rotavirus, Inactivated1.00relative potency1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Glass Vial 20 x 1.0 Dose
- Glass Vial 10 x 1.0 Dose
- Glass Vial 2 x 1.0 Dose
- Plastic Vial 1 x 50.0 Dose
- Glass Vial 1 x 50.0 Dose
- Plastic Vial 24 x 25.0 Dose
- Glass Vial 24 x 25.0 Dose
- Plastic Vial 12 x 25.0 Dose
- Glass Vial 12 x 25.0 Dose
- Plastic Vial 1 x 25.0 Dose
- Glass Vial 1 x 25.0 Dose
- Plastic Vial 10 x 5.0 Dose
- Glass Vial 10 x 5.0 Dose
- Plastic Vial 5 x 5.0 Dose
- Glass Vial 5 x 5.0 Dose
- Plastic Vial 1 x 5.0 Dose
- Glass Vial 1 x 5.0 Dose
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:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0177/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
Finland
-
France
-
Germany
-
Greece
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Portugal
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?: