Hiprabovis-4 suspensão injectável para bovinos vacina mista en suspensão injectável após reconstituição do liofilizado na componente líquida para bovinos adultos e vitelos.
Hiprabovis-4 suspensão injectável para bovinos vacina mista en suspensão injectável após reconstituição do liofilizado na componente líquida para bovinos adultos e vitelos.
Authorised
- Bovine herpesvirus 1, type 1, Inactivated
- Bovine parainfluenza virus 3, Inactivated
- Bovine viral diarrhoea virus 1, Inactivated
- Bovine respiratory syncytial virus, strain Lym-56, Live
Product identification
Medicine name:
Hiprabovis-4 suspensão injectável para bovinos vacina mista en suspensão injectável após reconstituição do liofilizado na componente líquida para bovinos adultos e vitelos.
Active substance:
- Bovine herpesvirus 1, type 1, Inactivated
- Bovine parainfluenza virus 3, Inactivated
- Bovine viral diarrhoea virus 1, Inactivated
- Bovine respiratory syncytial virus, strain Lym-56, Live
Target species:
-
Cattle (calf)
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Bovine herpesvirus 1, type 1, Inactivated50.00/enzyme-linked immunosorbent assay unit3.00millilitre(s)
-
Bovine parainfluenza virus 3, Inactivated
-
Bovine viral diarrhoea virus 1, Inactivated50.00/enzyme-linked immunosorbent assay unit3.00millilitre(s)
-
Bovine respiratory syncytial virus, strain Lym-56, Live100000.00/50% cell culture infectious dose3.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AH
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- Available only in Portuguese
- Available only in Portuguese
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:
- Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 562/96DGV
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 20/06/2023
Updated on: 26/06/2023