Veterinary Medicines Information website

Calcium S 50 aniMedica, otopina za injekciju, za goveda, ovce, koze, svinje, pse i mačke

Authorised
  • Phosphorylcolamine
  • Magnesium chloride hexahydrate
  • Calcium borogluconate
  • Calcium hydroxide
  • Calcium gluconate
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Product identification

Medicine name:
Calcium S 50 aniMedica, otopina za injekciju, za goveda, ovce, koze, svinje, pse i mačke
Active substance:
  • Phosphorylcolamine
  • Magnesium chloride hexahydrate
  • Calcium borogluconate
  • Calcium hydroxide
  • Calcium gluconate
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Phosphorylcolamine
    6.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium chloride hexahydrate
    65.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium borogluconate
    429.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium hydroxide
    13.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium gluconate
    31.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Croatia
Available in:
  • Croatia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pasteur Filiala Filipesti S.A.
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/13-01/453
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.
Croatian (PDF)
Published on: 22/05/2024
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