Veterinary Medicines

Tetanusan 50% šķīdums injekcijām liellopiem, zirgiem un cūkām

Authorised
  • Calcium gluconate monohydrate
  • Magnesium chloride hexahydrate
  • Sodium glycerophosphate pentahydrate
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Product identification

Medicine name:
Tetanusan 50% šķīdums injekcijām liellopiem, zirgiem un cūkām
Active substance:
  • Calcium gluconate monohydrate
  • Magnesium chloride hexahydrate
  • Sodium glycerophosphate pentahydrate
Target species:
  • Pig
  • Horse
  • Cattle
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Calcium gluconate monohydrate
    440.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium chloride hexahydrate
    125.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium glycerophosphate pentahydrate
    20.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Subcutaneous use
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05XA30
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Available in:
  • Latvia
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:
  • Kon-Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bela-Pharm GmbH & Co. KG
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/09/0006
Date of authorisation status change:

Documents

Summary of Product Characteristics

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

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

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 18/12/2025
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