Bovalto Respi 3, Suspension for injection
Bovalto Respi 3, Suspension for injection
Authorised
- Bovine respiratory syncytial virus, strain BIO-24, Inactivated
- Bovine parainfluenza virus 3, strain BIO-23, Inactivated
- Mannheimia haemolytica, serotype A1, strain DSM 5283, Inactivated
Product identification
Medicine name:
Bovalto Respi 3, Suspension for injection
Bovalto Respi 3 Suspensie voor injectie
Bovalto Respi 3 Suspension injectable
Bovalto Respi 3 Injektionssuspension
Active substance:
- Bovine respiratory syncytial virus, strain BIO-24, Inactivated
- Bovine parainfluenza virus 3, strain BIO-23, Inactivated
- Mannheimia haemolytica, serotype A1, strain DSM 5283, Inactivated
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Bovine respiratory syncytial virus, strain BIO-24, Inactivated1.00relative potency1.00Dose
-
Bovine parainfluenza virus 3, strain BIO-23, Inactivated1.00relative potency1.00Dose
-
Mannheimia haemolytica, serotype A1, strain DSM 5283, Inactivated1.00relative potency1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Milk0hour
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AL
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Plastic Vial 10 x 5.0 Dose
- Glass Vial 10 x 5.0 Dose
- Plastic Vial 1 x 50.0 Dose
- Glass Vial 1 x 50.0 Dose
- Plastic Vial 1 x 25.0 Dose
- Glass Vial 1 x 25.0 Dose
- Plastic Vial 1 x 5.0 Dose
- Glass Vial 1 x 5.0 Dose
- Plastic Vial 10 x 5.0 Dose
- Glass Vial 10 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 Animal Health Belgium S.A.
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/0128/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
France
-
Germany
-
Greece
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Labelling
This document does not exist in this language (English). You can find it in another language below.
How useful was this page?: