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SURCALCE injekčný roztok

Authorised
  • Calcium gluconate
  • Calcium acetate
  • Magnesium hypophosphite hexahydrate
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Product identification

Medicine name:
SURCALCE injekčný roztok
Active substance:
  • Calcium gluconate
  • Calcium acetate
  • Magnesium hypophosphite hexahydrate
Target species:
  • Cattle
  • Horse
  • Sheep
  • Goat
  • Pig
Route of administration:
  • Subcutaneous use
  • Intravenous use

Product details

Active substance and strength:
  • Calcium gluconate
    465.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium acetate
    37.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium hypophosphite hexahydrate
    30.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Milk
        0
        day
      • 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:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Sanochemia Pharmazeutika AG
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/398/91-S
Date of authorisation status change:

Documents

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Slovak (PDF)
Published on: 19/01/2022
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