Veterinary Medicines

CALCIUM GLUCONAT 38 % Kon-Pharma oldatos injekció A.U.V.

Authorised
  • Magnesium chloride hexahydrate
  • Calcium gluconate monohydrate
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Product identification

Medicine name:
CALCIUM GLUCONAT 38 % Kon-Pharma oldatos injekció A.U.V.
Active substance:
  • Magnesium chloride hexahydrate
  • Calcium gluconate monohydrate
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
  • Horse
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Magnesium chloride hexahydrate
    6.00
    gram(s)
    /
    100.00
    millilitre(s)
  • Calcium gluconate monohydrate
    38.00
    gram(s)
    /
    100.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12CX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Hungary
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Kon-Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bela-Pharm GmbH & Co. KG
Responsible authority:
  • Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Hungarian (PDF)
Published on: 1/06/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Hungarian (PDF)
Published on: 1/06/2025
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