Ginseng-logoplex injekció
Ginseng-logoplex injekció
Authorised
- STROPHANTHUS GRATUS D3
- Symphytum officinale D1
- RUBIA TINCTORUM D6
- RHUS TOXICODENDRON D2
- Gelsemium sempervirens D1
- SOLANUM DULCAMARA D2
- CONIUM MACULATUM D2
- ANAMIRTA COCCULUS D2
- Bryonia D1
- ATROPA BELLA-DONNA D2
- ARNICA MONTANA D1
- ACONITUM NAPELLUS D2
- PANAX QUINQUEFOLIUS
Product identification
Medicine name:
Ginseng-logoplex injekció
Active substance:
- STROPHANTHUS GRATUS D3
- Symphytum officinale D1
- RUBIA TINCTORUM D6
- RHUS TOXICODENDRON D2
- Gelsemium sempervirens D1
- SOLANUM DULCAMARA D2
- CONIUM MACULATUM D2
- ANAMIRTA COCCULUS D2
- Bryonia D1
- ATROPA BELLA-DONNA D2
- ARNICA MONTANA D1
- ACONITUM NAPELLUS D2
- PANAX QUINQUEFOLIUS
Target species:
-
Cattle
-
Sheep
-
Goat
-
Horse
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
STROPHANTHUS GRATUS D30.50milligram(s)1.00millilitre(s)
-
Symphytum officinale D12.70milligram(s)1.00millilitre(s)
-
RUBIA TINCTORUM D62.70milligram(s)1.00millilitre(s)
-
RHUS TOXICODENDRON D22.70milligram(s)1.00millilitre(s)
-
Gelsemium sempervirens D12.70milligram(s)1.00millilitre(s)
-
SOLANUM DULCAMARA D22.70milligram(s)1.00millilitre(s)
-
CONIUM MACULATUM D22.70milligram(s)1.00millilitre(s)
-
ANAMIRTA COCCULUS D22.70milligram(s)1.00millilitre(s)
-
Bryonia D12.70milligram(s)1.00millilitre(s)
-
ATROPA BELLA-DONNA D22.70milligram(s)1.00millilitre(s)
-
ARNICA MONTANA D12.70milligram(s)1.00millilitre(s)
-
ACONITUM NAPELLUS D22.70milligram(s)1.00millilitre(s)
-
PANAX QUINQUEFOLIUS2.70milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Sheep
-
Goat
-
Horse
-
Pig
-
Dog
-
Cat
-
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Homeopathic medicinal products (Article 19 of Directive No 2001/82/EC)
Marketing authorisation holder:
- Medicus Partner Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
- Cefak KG
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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