Veterinary Medicine Information website

Calciject 40 + 3 Solution for Injection

Authorised
  • Calcium gluconate
  • Magnesium hypophosphite hexahydrate
  • Boric acid
Download as PDF

Product identification

Medicine name:
Calciject 40 + 3 Solution for Injection
Active substance:
  • Calcium gluconate
  • Magnesium hypophosphite hexahydrate
  • Boric acid
Target species:
  • Cattle
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Calcium gluconate
    332.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium hypophosphite hexahydrate
    30.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Boric acid
    68.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • 400 ml polypropylene container sealed with bromobutyl bung (grey) and aluminium cap.
  • 400 ml Type III glass vial (amber) which is sealed using rubber wads (black) and aluminium screw cap

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/032/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 26/08/2024
Download