Porcilis Begonia DF Suspension for intamuscular injection
Porcilis Begonia DF Suspension for intamuscular injection
Authorised
- Aujeszky's disease virus, strain Begonia gE- tk-, Live
Product identification
Medicine name:
Porcilis Begonia DF Suspension for intamuscular injection
Porcilis Begonia Diluvac Forte Lyofilisaat en oplosmiddel voor suspensie voor injectie
Porcilis Begonia Diluvac Forte Lyophilisat et solvant pour suspension injectable
Porcilis Begonia Diluvac Forte Lyophilisat und Lösungsmittel zur Herstellung einer Injektionssuspension
Active substance:
- Aujeszky's disease virus, strain Begonia gE- tk-, Live
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Aujeszky's disease virus, strain Begonia gE- tk-, Live3162280.00/tissue culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AD01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- (ID12): 1 Box with 10 Box with (1 Bottle (Glass) with 100 Dose and 1 Bottle (Glass) with 200 millilitre(s)) (1000.0 Dose, 2000.0 millilitre(s))
- (ID11): 1 Box with 5 Box with (1 Bottle (Glass) with 100 Dose and 1 Bottle (Glass) with 200 millilitre(s)) (500.0 Dose, 1000.0 millilitre(s))
- (ID10): 1 Box with (1 Bottle (Glass) with 100 Dose and 1 Bottle (Glass) with 200 millilitre(s)) (100.0 Dose, 200.0 millilitre(s))
- (ID9): 1 Box with 10 Box with (1 Bottle (Glass) with 50 Dose and 1 Bottle (Glass) with 100 millilitre(s)) (500.0 Dose, 1000.0 millilitre(s))
- (ID8): 1 Box with 5 Box with (1 Bottle (Glass) with 50 Dose and 1 Bottle (Glass) with 100 millilitre(s)) (250.0 Dose, 500.0 millilitre(s))
- (ID7): 1 Box with (1 Bottle (Glass) with 50 Dose and 1 Bottle (Glass) with 100 millilitre(s)) (50.0 Dose, 100.0 millilitre(s))
- (ID6): 1 Box with 10 Box with (1 Bottle (Glass) with 25 Dose and 1 Bottle (Glass) with 50 millilitre(s)) (250.0 Dose, 500.0 millilitre(s))
- (ID5): 1 Box with 5 Box with (1 Bottle (Glass) with 25 Dose and 1 Bottle (Glass) with 50 millilitre(s)) (125.0 Dose, 250.0 millilitre(s))
- (ID4): 1 Box with (1 Bottle (Glass) with 25 Dose and 1 Bottle (Glass) with 50 millilitre(s)) (25.0 Dose, 50.0 millilitre(s))
- (ID3): 1 Box with 10 Box with (1 Bottle (Glass) with 10 Dose and 1 Bottle (Glass) with 20 millilitre(s)) (100.0 Dose, 200.0 millilitre(s))
- (ID2): 1 Box with 5 Box with (1 Bottle (Glass) with 10 Dose and 1 Bottle (Glass) with 20 millilitre(s)) (50.0 Dose, 100.0 millilitre(s))
- (ID1): 1 Box with (1 Bottle (Glass) with 10 Dose and 1 Bottle (Glass) with 20 millilitre(s)) (10.0 Dose, 20.0 millilitre(s))
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- FAMHP
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0012/001
Concerned member states:
-
Belgium
-
France
-
Greece
-
Italy
-
Luxembourg
-
Netherlands
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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