Lactovac Suspension for injection
Lactovac Suspension for injection
Not authorised
- Bovine rotavirus, strain 1005/78, Inactivated
- Bovine rotavirus, strain Holland, Inactivated
- Bovine coronavirus, strain 800, Inactivated
- Escherichia coli, serotype O9:K35 (fimbrial adhesin F5 and F41), strain S1091/83, Inactivated
Product identification
Medicine name:
Lactovac Suspension for injection
Lactovac Suspensie voor injectie
Lactovac Suspension injectable
Lactovac Injektionssuspension
Active substance:
- Bovine rotavirus, strain 1005/78, Inactivated
- Bovine rotavirus, strain Holland, Inactivated
- Bovine coronavirus, strain 800, Inactivated
- Escherichia coli, serotype O9:K35 (fimbrial adhesin F5 and F41), strain S1091/83, Inactivated
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Bovine rotavirus, strain 1005/78, Inactivated1.00relative potency1.00Dose
-
Bovine rotavirus, strain Holland, Inactivated1.00relative potency1.00Dose
-
Bovine coronavirus, strain 800, Inactivated1.00relative potency1.00Dose
-
Escherichia coli, serotype O9:K35 (fimbrial adhesin F5 and F41), strain S1091/83, Inactivated1.00relative potency1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal0day
-
Milk0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Type I glass vial containing 5 ml. The glass vial is closed with a type I rubber stopper, sealed with an aluminium crimp cap. Cardboard box with 10 glass vials of 1 dose (5 ml).
- Type I glass vial containing 25 ml. The glass vial is closed with a type I rubber stopper, sealed with an aluminium crimp cap. Cardboard box with 1 glass vial of 5 doses (25 ml).
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:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- FAMHP
Authorisation number:
- BE-V567084
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0417/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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