Veterinary Medicines

PROGRESSIS EMULSION FOR INJECTION FOR PIGS (SOWS AND GILTS)

Authorised
  • Porcine reproductive and respiratory syndrome virus, type 1, strain P120, Inactivated
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Product identification

Medicine name:
PROGRESSIS EMULSION FOR INJECTION FOR PIGS (SOWS AND GILTS)
Progressis Emulsie voor injectie
Progressis Emulsion injectable
Progressis Emulsion zur Injektion
Active substance:
  • Porcine reproductive and respiratory syndrome virus, type 1, strain P120, Inactivated
Target species:
  • Pig (for reproduction)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Porcine reproductive and respiratory syndrome virus, type 1, strain P120, Inactivated
    2.50
    log10 immunofluorescence unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (for reproduction)
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AA05
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Package description:
  • Box of 1 bottle of 5 doses
  • Box of 10 plastic bottles of 50 doses
  • Box of 1 plastic bottle of 50 doses
  • Box of 10 bottles of 25 doses
  • Box of 1 bottle of 25 doses
  • Box of 10 bottles of 10 doses
  • Box of 1 bottle of 10 doses
  • Box of 10 bottles of 5 doses

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva-Phylaxia Zrt.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0115/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • Finland
  • Germany
  • Greece
  • Ireland
  • Italy
  • Luxembourg
  • Netherlands
  • Portugal
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 7/06/2024
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French (PDF)
Published on: 7/06/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 7/06/2024
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French (PDF)
Published on: 7/06/2024
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German (PDF)
Published on: 7/06/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 7/06/2024
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French (PDF)
Published on: 7/06/2024
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German (PDF)
Published on: 7/06/2024
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