Veterinary Medicines

PHOSPHOR-HOMACCORD, injekcinis tirpalas

Authorised
  • PARIS QUADRIFOLIA D200
  • PARIS QUADRIFOLIA D30
  • PARIS QUADRIFOLIA D10
  • PARIS QUADRIFOLIA D6
  • ARGENTUM NITRICUM D200
  • ARGENTUM NITRICUM D30
  • ARGENTUM NITRICUM D10
  • PHOSPHORUS D200
  • PHOSPHORUS D30
  • PHOSPHORUS D10
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Product identification

Medicine name:
PHOSPHOR-HOMACCORD, injekcinis tirpalas
Active substance:
  • PARIS QUADRIFOLIA D200
  • PARIS QUADRIFOLIA D30
  • PARIS QUADRIFOLIA D10
  • PARIS QUADRIFOLIA D6
  • ARGENTUM NITRICUM D200
  • ARGENTUM NITRICUM D30
  • ARGENTUM NITRICUM D10
  • PHOSPHORUS D200
  • PHOSPHORUS D30
  • PHOSPHORUS D10
Target species:
  • Horse
  • Cattle
  • Pig
  • Sheep
  • Goat
  • Dog
  • Cat
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • PARIS QUADRIFOLIA D200
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • PARIS QUADRIFOLIA D30
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • PARIS QUADRIFOLIA D10
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • PARIS QUADRIFOLIA D6
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • ARGENTUM NITRICUM D200
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • ARGENTUM NITRICUM D30
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • ARGENTUM NITRICUM D10
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • PHOSPHORUS D200
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • PHOSPHORUS D30
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
  • PHOSPHORUS D10
    0.02
    millilitre(s)
    /
    1.00
    Ampoule
Pharmaceutical form:
  • Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QV03
Legal status of supply:
This information is not available for this product.
Authorisation status:
  • Valid
Authorised in:
  • Lithuania
Available in:
  • Lithuania
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:
  • Biologische Heilmittel Heel GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biologische Heilmittel Heel GmbH
Responsible authority:
  • State Food And Veterinary Service
Authorisation number:
  • LT/2/03/1538/001-002
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Lithuanian (PDF)
Published on: 29/02/2024
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