Veterinary Medicines

Larynx/Levisticum comp. PlantaVet

Authorised
  • NERVUS LARYNGEUS RECURRENS BOVIS GL DIL. D5 (HAB, VS. 41A)
  • NERVUS LARYNGEUS SUPERIOR BOVIS GL DIL. D5 (HAB, VS. 41A)
  • LARYNX BOVIS GL DIL. D5 (HAB, VS. 41B)
  • NERVUS VAGUS BOVIS GL DIL. D5 (HAB, VS. 41A)
  • Levisticum officinale D5
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Product identification

Medicine name:
Larynx/Levisticum comp. PlantaVet
Active substance:
  • NERVUS LARYNGEUS RECURRENS BOVIS GL DIL. D5 (HAB, VS. 41A)
  • NERVUS LARYNGEUS SUPERIOR BOVIS GL DIL. D5 (HAB, VS. 41A)
  • LARYNX BOVIS GL DIL. D5 (HAB, VS. 41B)
  • NERVUS VAGUS BOVIS GL DIL. D5 (HAB, VS. 41A)
  • Levisticum officinale D5
Target species:
  • Horse
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • NERVUS LARYNGEUS RECURRENS BOVIS GL DIL. D5 (HAB, VS. 41A)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • NERVUS LARYNGEUS SUPERIOR BOVIS GL DIL. D5 (HAB, VS. 41A)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • LARYNX BOVIS GL DIL. D5 (HAB, VS. 41B)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • NERVUS VAGUS BOVIS GL DIL. D5 (HAB, VS. 41A)
    1.00
    gram(s)
    /
    10.00
    millilitre(s)
  • Levisticum officinale D5
    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
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
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:
  • 6442763.00.00
Date of authorisation status change: