HIPRABOVIS-4 ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
HIPRABOVIS-4 ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Authorised
- Infectious Bovine rhinotracheitis virus, strain LA, Inactivated
- Bovine parainfluenza virus 3, strain SF-4, Inactivated
- Bovine viral diarrhoea virus, strain NADL, Inactivated
- Bovine respiratory syncytial virus, strain Lym-56, Live
Product identification
Medicine name:
HIPRABOVIS-4 ΕΝΕΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Active substance:
- Infectious Bovine rhinotracheitis virus, strain LA, Inactivated
- Bovine parainfluenza virus 3, strain SF-4, Inactivated
- Bovine viral diarrhoea virus, strain NADL, Inactivated
- Bovine respiratory syncytial virus, strain Lym-56, Live
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Infectious Bovine rhinotracheitis virus, strain LA, Inactivated10000000.00tissue culture infective dose 501.35millilitre(s)
-
Bovine parainfluenza virus 3, strain SF-4, Inactivated1000000.00tissue culture infective dose 500.75millilitre(s)
-
Bovine viral diarrhoea virus, strain NADL, Inactivated1000000.00tissue culture infective dose 500.60millilitre(s)
-
Bovine respiratory syncytial virus, strain Lym-56, Live100000.00tissue culture infective dose 501.00Tablet
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal21day
-
-
Subcutaneous use
- Cattle
-
Meat and offal21day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AH
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 35067/18-10-1999/K-0114301
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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