Porsilis Strepsuis
Porsilis Strepsuis
Authorised
- Streptococcus suis, serotype 2, strain P 1/7, Inactivated
Product identification
Medicine name:
Porsilis Strepsuis
Porcilis Strepsuis
Active substance:
- Streptococcus suis, serotype 2, strain P 1/7, Inactivated
Target species:
-
Pig (piglet)
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Streptococcus suis, serotype 2, strain P 1/7, Inactivated
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig (piglet)
-
Meat and offal0day
-
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- 100 ml (50 dose presentation) vials of glass Type I (Ph. Eur.) closed with a halogenobutyl rubber stopper and sealed with coded aluminium cap
- 50 ml (25 dose presentation) vials of glass Type I (Ph. Eur.) closed with a halogenobutyl rubber stopper and sealed with coded aluminium cap
- 20 ml (10 dose presentation) vials of glass Type I (Ph. Eur.) closed with a halogenobutyl rubber stopper and sealed with coded aluminium cap
- 100 ml (50 dose presentation) vials of PET closed with a halogenobutyl rubber stopper and sealed with coded aluminium cap
- 50 ml (25 dose presentation) vials of PET closed with a halogenobutyl rubber stopper and sealed with coded aluminium cap
- 20 ml (10 dose presentation) vials of PET closed with a halogenobutyl rubber stopper and sealed with coded aluminium cap
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:
- MSD Animal Health Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- R713/02 DGV
Date of authorisation status change:
Reference member state:
-
Italy
Procedure number:
- IT/V/0110/001
Concerned member states:
-
Greece
-
Portugal
-
Spain
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: 16/02/2022
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