Veterinary Medicines

VITAMIN-K/AGROSEED CANDILIDIS ενέσιμο διάλυμα 10 mg/ml για ιπποειδή, βοοειδή, μόσχους, χοίρους, σκύλο, γάτα

Authorised
  • Menadione sodium bisulfite
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Product identification

Medicine name:
VITAMIN-K/AGROSEED CANDILIDIS ενέσιμο διάλυμα 10 mg/ml για ιπποειδή, βοοειδή, μόσχους, χοίρους, σκύλο, γάτα
Active substance:
  • Menadione sodium bisulfite
Target species:
  • Cattle
  • Equid
  • Cattle (calf)
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular and intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Menadione sodium bisulfite
    10.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular and intravenous use
    • Cattle
      • Meat and offal, milk
        0
        day
    • Equid
      • Meat and offal, milk
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Dog
      • Not applicable
        no withdrawal period
    • Cat
      • Not applicable
        no withdrawal period
  • Subcutaneous use
    • Cattle
      • Meat and offal, milk
        0
        day
    • Equid
      • Meat and offal, milk
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Dog
      • Not applicable
        no withdrawal period
    • Cat
      • Not applicable
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB02BA
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Greece
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Candilidis S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Alfasan International B.V.
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 37813/05-05-2021/K-0130001
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Greek (PDF)
Published on: 23/06/2023
Updated on: 27/06/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Greek (PDF)
Published on: 23/06/2023
Updated on: 27/06/2023
Download