Veterinary Medicines

Calciovet oldatos injekció A.U.V.

Authorised
  • Calcium saccharate
  • Sodium hypophosphite
  • CALCIUM GLUCOHEPTONATE
  • Calcium gluconate
  • Magnesium chloride hexahydrate
Download as PDF

Product identification

Medicine name:
Calciovet oldatos injekció A.U.V.
Active substance:
  • Calcium saccharate
  • Sodium hypophosphite
  • CALCIUM GLUCOHEPTONATE
  • Calcium gluconate
  • Magnesium chloride hexahydrate
Target species:
  • Cattle
  • Sheep
  • Dog
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Calcium saccharate
    10.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium hypophosphite
    30.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • CALCIUM GLUCOHEPTONATE
    45.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium gluconate
    190.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium chloride hexahydrate
    60.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Dog
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Hungary
Available in:
  • Hungary
Package description:

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:
  • Divasa Farmavic S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Divasa Farmavic S.A.
Responsible authority:
  • Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
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."