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Veterinary Medicines

CHELIDONIUM -HOMACCORD VETERINARIO

Authorised
  • ATROPA BELLA-DONNA D10
  • ATROPA BELLA-DONNA D1000
  • ATROPA BELLA-DONNA D200
  • ATROPA BELLA-DONNA D30
  • ATROPA BELLA-DONNA D4
  • CHELIDONIUM MAJUS D10
  • CHELIDONIUM MAJUS D200
  • FEL TAURI D10
  • FEL TAURI D200

Product identification

Medicine name:
CHELIDONIUM -HOMACCORD VETERINARIO
Active substance:
  • ATROPA BELLA-DONNA D10
  • ATROPA BELLA-DONNA D1000
  • ATROPA BELLA-DONNA D200
  • ATROPA BELLA-DONNA D30
  • ATROPA BELLA-DONNA D4
  • CHELIDONIUM MAJUS D10
  • CHELIDONIUM MAJUS D200
  • FEL TAURI D10
  • FEL TAURI D200
Target species:
  • Cattle (cow)
  • Cattle
  • Ornamental bird
  • Dog
  • Goat
  • Sheep (ewe)
  • Sheep
  • Horse
  • Cat
  • Rabbit
  • Fish
  • Rodents
  • Pig
Route of administration:
  • Oral use
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • ATROPA BELLA-DONNA D10
    15.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • ATROPA BELLA-DONNA D1000
    15.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • ATROPA BELLA-DONNA D200
    15.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • ATROPA BELLA-DONNA D30
    15.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • ATROPA BELLA-DONNA D4
    15.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • CHELIDONIUM MAJUS D10
    30.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • CHELIDONIUM MAJUS D200
    30.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • FEL TAURI D10
    5.00
    milligram(s)
    /
    5.00
    millilitre(s)
  • FEL TAURI D200
    5.00
    milligram(s)
    /
    5.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Homeopathic Registration
Marketing authorisation holder:
  • Biologische Heilmittel Heel GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biologische Heilmittel Heel GmbH
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 3/06/2022