Larynx/Apis comp. PlantaVet
Larynx/Apis comp. PlantaVet
Authorised
- Levisticum officinale D14
- BRYONIA CRETICA FERM 33B DIL. D14
- APIS MELLIFICA EX ANIMALE TOTO GL DIL. D16 (HAB, VS. 41C)
- NERVUS VAGUS BOVIS GL DIL. D16 (HAB, VS. 41A)
- NERVUS LARYNGEUS SUPERIOR BOVIS GL DIL. D16 (HAB, VS. 41A)
- NERVUS LARYNGEUS RECURRENS BOVIS GL DIL. D16 (HAB, VS. 41A)
- LARYNX BOVIS GL DIL. D16 (HAB, VS. 41B)
Product identification
Medicine name:
Larynx/Apis comp. PlantaVet
Active substance:
- Levisticum officinale D14
- BRYONIA CRETICA FERM 33B DIL. D14
- APIS MELLIFICA EX ANIMALE TOTO GL DIL. D16 (HAB, VS. 41C)
- NERVUS VAGUS BOVIS GL DIL. D16 (HAB, VS. 41A)
- NERVUS LARYNGEUS SUPERIOR BOVIS GL DIL. D16 (HAB, VS. 41A)
- NERVUS LARYNGEUS RECURRENS BOVIS GL DIL. D16 (HAB, VS. 41A)
- LARYNX BOVIS GL DIL. D16 (HAB, VS. 41B)
Target species:
-
Horse
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Levisticum officinale D141.00gram(s)10.00millilitre(s)
-
BRYONIA CRETICA FERM 33B DIL. D141.00gram(s)10.00millilitre(s)
-
APIS MELLIFICA EX ANIMALE TOTO GL DIL. D16 (HAB, VS. 41C)1.00gram(s)10.00millilitre(s)
-
NERVUS VAGUS BOVIS GL DIL. D16 (HAB, VS. 41A)1.00gram(s)10.00millilitre(s)
-
NERVUS LARYNGEUS SUPERIOR BOVIS GL DIL. D16 (HAB, VS. 41A)1.00gram(s)10.00millilitre(s)
-
NERVUS LARYNGEUS RECURRENS BOVIS GL DIL. D16 (HAB, VS. 41A)1.00gram(s)10.00millilitre(s)
-
LARYNX BOVIS GL DIL. D16 (HAB, VS. 41B)1.00gram(s)10.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- Available only in German
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
- Wala-Heilmittel GmbH
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 6442823.00.00
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?: