Veterinary Medicines

VIMCO emulsion for injection for ewes and female goats

Authorised
  • Staphylococcus aureus, strain SP 140, Inactivated
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Product identification

Medicine name:
VIMCO emulsion for injection for ewes and female goats
VIMCO ενέσιμο γαλάκτωμα για προβατίνες και θηλυκές αίγες
Active substance:
  • Staphylococcus aureus, strain SP 140, Inactivated
Target species:
  • Sheep (ewe)
  • Goat (adult female)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Staphylococcus aureus, strain SP 140, Inactivated
    8.98
    cells
    /
    1.00
    Dose
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Sheep (ewe)
      • Meat and offal
        0
        day
    • Goat (adult female)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI03AB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Cyprus
Package description:
  • box containing 1 PET vial containing 50 doses (100 ml)
  • box containing 1 PET vial containing 25 doses (50 ml)
  • box containing 1 PET vial containing 5 doses (10 ml)
  • box containing 1 glass vial containing 50 doses (100 ml)
  • box containing 1 glass vial containing 25 doses (50 ml)
  • box containing 1 glass vial containing 5 doses (10 ml)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Hipra S.A.
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • CY00965V
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0209/001
Concerned member states:
  • Belgium
  • Bulgaria
  • Cyprus
  • France
  • Germany
  • Greece
  • Ireland
  • Italy
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 24/07/2025
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Greek (PDF)
Published on: 12/12/2023
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Summary of Product Characteristics

English (PDF)
Published on: 21/12/2023
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Package Leaflet

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

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