Veterinary Medicines

Porcilis Ery+Parvo Suspension for injection

Authorised
  • Erysipelothrix rhusiopathiae, serotype 2, strain M2, Inactivated
  • Porcine parvovirus, strain 014, Inactivated
Download as PDF

Product identification

Medicine name:
Porcilis Ery + Parvo suspensão injetável para porcos
Porcilis Ery+Parvo Suspension for injection
Active substance:
  • 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 2, strain M2, Inactivated
    1.00
    Protective Dose
    /
    2.00
    millilitre(s)
  • Porcine parvovirus, strain 014, Inactivated
    552.00
    enzyme-linked immunosorbent assay unit
    /
    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:
This information is not available for this product.
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:
  • 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:
  • R745/05 DGV
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0233/001
Concerned member states:
  • Norway
  • Portugal

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."