Lachesis D8, Flüssige Verdünnung zur Injektion
  • LACHESIS MUTUS DIL. D8
  • Valid
Authorised in these countries:
  • Germany
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Product identification

Medicine name:
Lachesis D8, Flüssige Verdünnung zur Injektion
Active substance and strength:
  • LACHESIS MUTUS DIL. D8
Anatomical therapeutic chemical veterinary (ATCvet) codes:
This information is not available for this product.
Authorisation number:
  • 31951.00.00
Product identification number:
  • 8092201e-d7d7-44df-89c6-5cf5de111f42
Permanent identification number:
  • 600000100061

Product details

Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Dog
    • Goat
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Cat
    • Pig
      • Meat and offal
        0
        day
    • Pig (sucking piglet)
      • Meat and offal
        0
        day

Availability

Package description:
Manufacturing sites for batch release:
This information is not available for this product.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Homeopathic Registration
Procedure number:
  • 2131951
Date of authorisation status change:
Legal basis of product authorisation:
This information is not available for this product.
Authorisation country:
  • Germany
Responsible authority:
  • BVL
Marketing authorisation holder:
  • Ziegler GmbH Homoeopathika Ad Us. Vet.
Marketing authorisation issued:
Reference member state:
This information is not available for this product.
Concerned member states:
This information is not available for this product.
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

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