Veterinary Medicines

Porcilis Begonia DF Suspension for intamuscular injection

Authorised
  • Aujeszky's disease virus, strain Begonia gE- tk-, Live
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Product identification

Medicine name:
Porcilis Begonia DF Suspension for intamuscular 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-, Live
    316228.00
    50% tissue culture infectious dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AD01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Luxembourg
Package description:
  • (ID12) 1000 Dose; 2000 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 100 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 200 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID11) 500 Dose; 1000 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 100 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Glass) with 200 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID10) 100 Dose; 200 millilitre(s): Box (Cardboard) with 1 Bottle (Glass type I) with 100 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 200 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID9) 500 Dose; 1000 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 50 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 100 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID8) 250 Dose; 500 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 50 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 100 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID7) 50 Dose; 100 millilitre(s): Box (Cardboard) with 1 Bottle (Glass type I) with 50 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 100 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID6) 250 Dose; 500 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 25 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 50 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID5) 125 Dose; 250 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 25 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 50 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID4) 25 Dose; 50 millilitre(s): Box (Cardboard) with 1 Bottle (Glass type I) with 25 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 50 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID3) 100 Dose; 200 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 10 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 20 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID2) 50 Dose; 100 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 10 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 20 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID1) 10 Dose; 20 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 10 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Glass) with 20 millilitre(s), closed with Kappe and Stopfen (Aluminium, Butylkautschuk)
  • (ID24) 1000 Dose; 2000 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 100 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 200 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID23) 500 Dose; 1000 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 100 Dose, closed with Kappe and Stopfen (Aluminium, Halobutyl Rubber) and 1 Bottle (Polyethylenterephthalat) with 200 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID22) 100 Dose; 200 millilitre(s): Box (Cardboard) with 1 Bottle (Glass type I) with 100 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 200 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID21) 500 Dose; 1000 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 50 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 100 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID20) 250 Dose; 500 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 50 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 100 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID19) 50 Dose; 100 millilitre(s): Box (Cardboard) with 1 Bottle (Glass type I) with 50 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 100 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID18) 250 Dose; 500 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 25 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 50 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID17) 125 Dose; 250 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 25 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 50 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID16) 25 Dose; 50 millilitre(s): Box (Cardboard) with 1 Bottle (Glass type I) with 25 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 50 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID15) 100 Dose; 200 millilitre(s): Box (Cardboard) with 10 Box (Cardboard) each with 1 Bottle (Glass type I) with 10 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 20 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID14) 50 Dose; 100 millilitre(s): Box (Cardboard) with 5 Box (Cardboard) each with 1 Bottle (Glass type I) with 10 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 20 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, Aluminium)
  • (ID13) 10 Dose; 20 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 10 Dose, closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium) and 1 Bottle (Polyethylenterephthalat) with 20 millilitre(s), closed with Stopfen and Kappe (Butylkautschuk, 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.
Responsible authority:
  • Ministry Of Health And Social Security
Authorisation number:
  • V 817/96/12/0544
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)

Documents

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Published on: 25/09/2025
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