Porcilis APP suspension for injection for pigs
Porcilis APP suspension for injection for pigs
Not authorised
- Actinobacillus pleuropneumoniae, Inactivated
- Actinobacillus pleuropneumoniae, outer membrane protein
- Actinobacillus pleuropneumoniae, APX I toxoid
- Actinobacillus pleuropneumoniae, APX II toxoid
- Actinobacillus pleuropneumoniae, APX III toxoid
Product identification
Medicine name:
Porcilis APP suspension for injection for pigs
Active substance:
- Actinobacillus pleuropneumoniae, Inactivated
- Actinobacillus pleuropneumoniae, outer membrane protein
- Actinobacillus pleuropneumoniae, APX I toxoid
- Actinobacillus pleuropneumoniae, APX II toxoid
- Actinobacillus pleuropneumoniae, APX III toxoid
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Actinobacillus pleuropneumoniae, Inactivated600.00milligram(s)1.00Dose
-
Actinobacillus pleuropneumoniae, outer membrane protein50.00unit(s)1.00Dose
-
Actinobacillus pleuropneumoniae, APX I toxoid50.00unit(s)1.00Dose
-
Actinobacillus pleuropneumoniae, APX II toxoid50.00unit(s)1.00Dose
-
Actinobacillus pleuropneumoniae, APX III toxoid50.00unit(s)1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Expired
Authorised in:
-
Luxembourg
Package description:
- Carton with one glass bottle type I (Ph. Eur.) or PET bottle with halogenated rubber stoppers and aluminium closures, containing 250 ml (125 doses).
- Carton with one glass bottle type I (Ph. Eur.) or PET bottle with halogenated rubber stoppers and aluminium closures, containing 100 ml (50 doses).
- Carton with one glass bottle type I (Ph. Eur.) or PET bottle with halogenated rubber stoppers and aluminium closures, containing 50 ml (25 doses).
- Carton with one glass bottle type I (Ph. Eur.) or PET bottle with halogenated rubber stoppers and aluminium closures, containing 20 ml (10 doses).
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Le Ministère De La Santé Division De La Pharmacie Et Des Médicaments
Authorisation number:
- V 817/98/11/0615
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0327/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 28/01/2022
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