Porcilis PARVO Vet., suspension for injection
Porcilis PARVO Vet., suspension for injection
Authorised
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
Product identification
Medicine name:
Porcilis PARVO Vet., suspension for injection
Porcilis Parvo Vet. injektionsvæske, suspension
Active substance:
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
- Porcine parvovirus, strain 014, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Porcine parvovirus, strain 014, Inactivated552.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Porcine parvovirus, strain 014, Inactivated552.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Porcine parvovirus, strain 014, Inactivated552.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Porcine parvovirus, strain 014, Inactivated552.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Porcine parvovirus, strain 014, Inactivated552.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Porcine parvovirus, strain 014, Inactivated552.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 14729
Date of authorisation status change:
Reference member state:
-
Denmark
Procedure number:
- DK/V/0106/001
Concerned member states:
-
Austria
-
Finland
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
Danish (PDF)
Published on: 10/12/2025
PI.pdf
English (PDF)
Download Published on: 27/01/2022