Porcilis Ery Suspension for injection
Porcilis Ery Suspension for injection
Authorised
- Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
Product identification
Medicine name:
Porcilis Ery Suspension for injection
Porcilis Ery Injektionssuspension für Schweine
Active substance:
- Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated1.00/Protective Dose2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID6) 100 millilitre(s): Box with 1 Vial (Polyethylenterephthalat) with 100 millilitre(s), closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium)
- (ID2) 20 millilitre(s): Box with 1 Vial (Polyethylenterephthalat) with 20 millilitre(s), closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium)
- (ID8) 250 millilitre(s): Box with 1 Vial (Polyethylenterephthalat) with 250 millilitre(s), closed with Stopfen and Kappe (Halobutyl Rubber, Aluminium)
- (ID4) 50 millilitre(s): Box with 1 Vial (Polyethylenterephthalat) with 50 millilitre(s), closed with Stopfen and Kappe (Halobutyl Rubber, 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 Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- 57a/95
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0232/001
Concerned member states:
-
Norway
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 7/08/2025
German (PDF)
Published on: 15/08/2025