Veterinary Medicines

Procal Inj. Solution for injection for cattle, horses, calves, foals, sheep, goats, pigs, piglets, dogs, cats and rabbits

Authorised
  • CALCIUM GLUCOHEPTONATE
  • Calcium gluconate
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Product identification

Medicine name:
Procal Inj. инжекционен разтвор за говеда, коне, телета, кончета, овце, кози, прасета, прасенца, кучета, котки и зайци
Procal Inj. Solution for injection for cattle, horses, calves, foals, sheep, goats, pigs, piglets, dogs, cats and rabbits
Active substance:
  • CALCIUM GLUCOHEPTONATE
  • Calcium gluconate
Target species:
  • Cattle
  • Horse
  • Cattle (calf)
  • Horse (foal)
  • Sheep
  • Goat
  • Pig
  • Pig (piglet)
  • Dog
  • Cat
  • Rabbit
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • CALCIUM GLUCOHEPTONATE
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium gluconate
    350.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Horse (foal)
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Pig (piglet)
      • Meat and offal
        0
        day
    • Rabbit
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Kepro B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Kepro B.V.
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-1877
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Bulgarian (PDF)
Published on: 17/12/2024
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Labelling

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Bulgarian (PDF)
Published on: 17/12/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 17/12/2024
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