Veterinary Medicines

CALFORMAG, Injekční roztok

Not authorised
  • PHOSPHORUS
  • CALCIUM
  • MAGNESIUM
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Product identification

Medicine name:
CALFORMAG, Injekční roztok
Active substance:
  • PHOSPHORUS
  • CALCIUM
  • MAGNESIUM
Target species:
  • Cattle
  • Horse
  • Sheep
  • Goat
  • Pig
  • Dog
Route of administration:
  • Intravenous use
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • PHOSPHORUS
    10.10
    milligram(s)
    /
    1.00
    millilitre(s)
  • CALCIUM
    44.60
    milligram(s)
    /
    1.00
    millilitre(s)
  • MAGNESIUM
    6.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat
        0
        day
      • Milk
        0
        day
    • Horse
      • Meat
        0
        day
    • Sheep
      • Meat
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat
        0
        day
  • Subcutaneous use
    • Cattle
      • Meat
        0
        day
      • Milk
        0
        day
    • Horse
      • Meat
        0
        day
    • Sheep
      • Meat
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat
        0
        day
  • Intramuscular use
    • Cattle
      • Meat
        0
        day
      • Milk
        0
        day
    • Horse
      • Meat
        0
        day
    • Sheep
      • Meat
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Czechia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • BB Pharma a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Farmacia Martin a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicines
Authorisation number:
  • 96/002/02-C
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.
Czech (PDF)
Published on: 26/10/2022
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Package Leaflet

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Czech (PDF)
Published on: 26/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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