Suvaxyn® Parvo/E
Suvaxyn® Parvo/E
Not authorised
- Erysipelothrix rhusiopathiae, serotype 2, Inactivated
- Porcine parvovirus, strain S-80, Inactivated
Product identification
Medicine name:
Suvaxyn® Parvo/E
Active substance:
- Erysipelothrix rhusiopathiae, serotype 2, Inactivated
- Porcine parvovirus, strain S-80, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Erysipelothrix rhusiopathiae, serotype 2, Inactivated13.50/relative potency2.00millilitre(s)
-
Porcine parvovirus, strain S-80, Inactivated94.10/haemagglutination inhibiting unit(s)2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Revoked
Authorised in:
-
Portugal
Package description:
- Available only in Portuguese
- Available only in Portuguese
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 8(3) of Directive No 2001/83/EC)
Marketing authorisation holder:
- Zoetis Portugal Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Portugal Lda.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- UPD 1.6.1-4 JSON NAP Chpt2 C2 Mandatory 889/01/15RIVPT
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet