Porsilis Ery+Parvo sospensione iniettabile per suini
Porsilis Ery+Parvo sospensione iniettabile per suini
Authorised
- Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
- Porcine parvovirus, strain 014, Inactivated
Product identification
Medicine name:
Porsilis Ery+Parvo sospensione iniettabile per suini
Active substance:
- Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
- Porcine parvovirus, strain 014, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Erysipelothrix rhusiopathiae, serotype 1, strain 1-203, Inactivated50.00/international unit(s)2.00millilitre(s)
-
Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated50.00/international unit(s)2.00millilitre(s)
-
Porcine parvovirus, strain 014, Inactivated9.00/log2 haemagglutination inhibiting unit(s)2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
-
-
Pig
-
Meat and offal0day
-
Unspecified0day
-
Meat and offal0day
-
Unspecified0day
-
Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
-
Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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Meat and offal0day
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Unspecified0day
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-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available in:
-
Italy
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
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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in another language below.
Italian (PDF)
Published on: 18/09/2024