Veterinary Medicines

Calciovet solução injetável

Authorised
  • Calcium gluconate
  • Calcium gluconoglucoheptonate
  • Magnesium clofibrate
  • Calcium saccharate
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Product identification

Medicine name:
Calciovet solução injetável
Active substance:
  • Calcium gluconate
  • Calcium gluconoglucoheptonate
  • Magnesium clofibrate
  • Calcium saccharate
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Calcium gluconate
    190.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium gluconoglucoheptonate
    45.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium clofibrate
    60.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium saccharate
    10.00
    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
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Dog
    • Cat
  • Intravenous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
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:
  • Divasa Farmavic S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Divasa Farmavic S.A.
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 51185
Date of authorisation status change:

Documents

Combined File of all Documents

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Portuguese (PDF)
Published on: 20/06/2023
Updated on: 26/06/2023
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