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Veterinary Medicines

Tendo/Allium comp. PlantaVet

Authorised
  • ALLIUM CEPA FERM 34A DIL. D7
  • VAGINAE SYNOVIALES TENDINUM BOVIS GL DIL. D16 (HAB, VS. 41C)
  • PERIOSTEUM BOVIS GL DIL. D16 (HAB, VS. 41B)
  • TENDO BOVIS GL DIL. D16 (HAB, VS. 41B)
  • Arnica montana ex planta tota D5
  • SYMPHYTUM OFFICINALE D5
  • Stannum metallicum D14

Product identification

Medicine name:
Tendo/Allium comp. PlantaVet
Active substance:
  • ALLIUM CEPA FERM 34A DIL. D7
  • VAGINAE SYNOVIALES TENDINUM BOVIS GL DIL. D16 (HAB, VS. 41C)
  • PERIOSTEUM BOVIS GL DIL. D16 (HAB, VS. 41B)
  • TENDO BOVIS GL DIL. D16 (HAB, VS. 41B)
  • Arnica montana ex planta tota D5
  • SYMPHYTUM OFFICINALE D5
  • Stannum metallicum D14
Target species:
  • Horse
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • ALLIUM CEPA FERM 34A DIL. D7
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • VAGINAE SYNOVIALES TENDINUM BOVIS GL DIL. D16 (HAB, VS. 41C)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • PERIOSTEUM BOVIS GL DIL. D16 (HAB, VS. 41B)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • TENDO BOVIS GL DIL. D16 (HAB, VS. 41B)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • Arnica montana ex planta tota D5
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • SYMPHYTUM OFFICINALE D5
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • Stannum metallicum D14
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Subcutaneous use
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • SaluVet GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Wala-Heilmittel GmbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 6500101.00.00
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 24/02/2025