Veterinary Medicine Information website

Calciovet oldatos injekció A.U.V.

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

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
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Authorisation status:
  • Valid
Authorised in:
  • Hungary
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
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: