Veterinary Medicines

Miktiolith ReVet RV 18 - Globuli für Tiere

Authorised
  • Berberis vulgaris C4
  • LYTTA VESICATORIA C6
  • LYCOPODIUM CLAVATUM C9
  • Sabal serrulata C4
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Product identification

Medicine name:
Miktiolith ReVet RV 18 - Globuli für Tiere
Active substance:
  • Berberis vulgaris C4
  • LYTTA VESICATORIA C6
  • LYCOPODIUM CLAVATUM C9
  • Sabal serrulata C4
Target species:
  • Cattle
  • Cattle (calf)
  • Dog
  • Goat
  • Sheep
  • Horse
  • Cat
  • Rabbit
  • Ferret
  • Small rodents
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Berberis vulgaris C4
    2.50
    milligram(s)
    /
    1.00
    gram(s)
  • LYTTA VESICATORIA C6
    2.50
    milligram(s)
    /
    1.00
    gram(s)
  • LYCOPODIUM CLAVATUM C9
    2.50
    milligram(s)
    /
    1.00
    gram(s)
  • Sabal serrulata C4
    2.50
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Pillules
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Dog
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Cat
    • Rabbit
      • Meat and offal
        0
        day
    • Ferret
    • Small rodents
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QV03AX
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:

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:
  • Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-30032
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: 2/01/2014
Updated on: 9/07/2024
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 18/06/2018
Updated on: 9/07/2024
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 2/01/2014
Updated on: 9/07/2024
Download
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