Veterinary Medicines

Porcilis Ery+Parvo Suspension for injection

Authorised
  • Porcine parvovirus, strain 014, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
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Product identification

Medicine name:
Porcilis Ery+Parvo Suspension for injection
Porcilis Ery + Parvo
Active substance:
  • Porcine parvovirus, strain 014, Inactivated
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Porcine parvovirus, strain 014, Inactivated
    552.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
    1.00
    Protective Dose
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:
  • (ID44) 250 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 250 millilitre(s)
  • (ID34) 100 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s)
  • (ID24) 50 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 50 millilitre(s)
  • (ID14) 20 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 20 millilitre(s)

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:
  • 59a/95
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0233/001
Concerned member states:
  • Norway
  • Portugal

Documents

Combined File of all Documents

English (PDF)
Published on: 27/06/2024
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