Porcilis Begonia Unisolve Suspension for intramuscular injection
Porcilis Begonia Unisolve Suspension for intramuscular injection
Authorised
- Aujeszky's disease virus, strain Begonia gE- tk-, Live
Product identification
Medicine name:
Porcilis Begonia Unisolve Suspension for intramuscular injection
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-, Live316228.00/50% tissue culture infectious dose1.00Dose
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) 500 Dose; 1000 millilitre(s): Box (cardboard) with 5 Bottle (Glass type I) each with 100 Dose, closed with Kappe (aluminium) and Stopper (Halobutyl Rubber) and 5 Bottle (Glass type II) each with 200 millilitre(s), closed with Kappe (aluminium) and Stopper (butyl rubber)
- (ID10) 125 Dose; 250 millilitre(s): Box (cardboard) with 5 Bottle (Glass type I) each with 25 Dose, closed with Kappe (aluminium) and Stopper (Halobutyl Rubber) and 5 Bottle (Glass type I) each with 50 millilitre(s), closed with Kappe (aluminium) and Stopper (butyl rubber)
- (ID11) 250 Dose; 500 millilitre(s): Box (cardboard) with 5 Bottle (Glass type I) each with 50 Dose, closed with Kappe (aluminium) and Stopper (Halobutyl Rubber) and 5 Bottle (Glass type II) each with 100 millilitre(s), closed with Kappe (aluminium) and Stopper (butyl rubber)
- (ID9) 50 Dose; 100 millilitre(s): Box (cardboard) with 5 Bottle (Glass type I) each with 10 Dose, closed with Kappe (aluminium) and Stopper (Halobutyl Rubber) and 5 Bottle (Glass type I) each with 20 millilitre(s), closed with Kappe (aluminium) and Stopper (butyl rubber)
- (ID1) 10 Dose; 20 millilitre(s): Box (cardboard) with 1 Bottle (Glass type I) with 10 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 1 Bottle (Glass type I) with 20 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
- (ID2) 100 Dose; 200 millilitre(s): Box (cardboard) with 10 Bottle (Glass type I) each with 10 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 10 Bottle (Glass type I) each with 20 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
- (ID3) 25 Dose; 50 millilitre(s): Box (cardboard) with 1 Bottle (Glass type I) with 25 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 1 Bottle (Glass type I) with 50 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
- (ID4) 250 Dose; 500 millilitre(s): Box (cardboard) with 10 Bottle (Glass type I) each with 25 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 10 Bottle (Glass type I) each with 50 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
- (ID5) 50 Dose; 100 millilitre(s): Box (cardboard) with 1 Bottle (Glass type I) with 50 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 1 Bottle (Glass type II) with 100 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
- (ID6) 500 Dose; 1000 millilitre(s): Box (cardboard) with 10 Bottle (Glass type II) each with 100 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium) and 10 Bottle (Glass type I) each with 50 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium)
- (ID7) 100 Dose; 200 millilitre(s): Box (cardboard) with 1 Bottle (Glass type I) with 100 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 1 Bottle (Glass type II) with 200 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
- (ID8) 1000 Dose; 2000 millilitre(s): Box (cardboard) with 10 Bottle (Glass type I) each with 100 Dose, closed with Stopper (Halobutyl Rubber) and Kappe (aluminium) and 10 Bottle (Glass type II) each with 200 millilitre(s), closed with Stopper (butyl rubber) and Kappe (aluminium)
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.
- Intervet International GmbH
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:
-
Germany
Procedure number:
- DE/V/0006/001
Concerned member states:
-
Belgium
-
France
-
Italy
-
Netherlands
-
Portugal
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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Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 7/05/2026