Veterinary Medicines

Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs

Authorised
  • CALCIUM GLUCONATE FOR INJECTION
  • Magnesium chloride hexahydrate
  • Sodium glycerophosphate pentahydrate
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Product identification

Medicine name:
Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan 250 mg/ml + 80 mg/ml + 10 mg/1 ml Roztwór do infuzji
Active substance:
  • CALCIUM GLUCONATE FOR INJECTION
  • Magnesium chloride hexahydrate
  • Sodium glycerophosphate pentahydrate
Target species:
  • Horse
  • Pig
  • Cattle
Route of administration:
  • Intravenous use

Product details

Active substance and strength:
  • CALCIUM GLUCONATE FOR INJECTION
    250.00
    milligram(s)/millilitre
    /
    1.00
    milligram(s)/millilitre
  • Magnesium chloride hexahydrate
    80.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium glycerophosphate pentahydrate
    10.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for infusion
Withdrawal period by route of administration:
  • Intravenous use
    • Horse
      • Milk
        5
        week
    • Pig
      • Meat and offal
        5
        week
    • Cattle
      • Milk
        5
        week
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
Package description:
  • Polypropylene (PP) bottles closed with a bromobutyl rubber stopper, type I and secured with an aluminium cap. Package size: 500 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 3171
Date of authorisation status change:
Reference member state:
  • Poland
Procedure number:
  • PL/V/0110/001
Concerned member states:
  • Bulgaria
  • Czechia
  • Greece
  • Hungary
  • Italy
  • Lithuania
  • Portugal
  • Romania
  • Spain

Documents

Summary of Product Characteristics

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Polish (PDF)
Published on: 18/12/2025
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Package Leaflet

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Polish (PDF)
Published on: 18/12/2025
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Labelling

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Polish (PDF)
Published on: 18/12/2025
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