PHOSPHOR-HOMACCORD, injekcinis tirpalas
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
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 D2000.02millilitre(s)1.00Ampoule
-
PARIS QUADRIFOLIA D300.02millilitre(s)1.00Ampoule
-
PARIS QUADRIFOLIA D100.02millilitre(s)1.00Ampoule
-
PARIS QUADRIFOLIA D60.02millilitre(s)1.00Ampoule
-
ARGENTUM NITRICUM D2000.02millilitre(s)1.00Ampoule
-
ARGENTUM NITRICUM D300.02millilitre(s)1.00Ampoule
-
ARGENTUM NITRICUM D100.02millilitre(s)1.00Ampoule
-
PHOSPHORUS D2000.02millilitre(s)1.00Ampoule
-
PHOSPHORUS D300.02millilitre(s)1.00Ampoule
-
PHOSPHORUS D100.02millilitre(s)1.00Ampoule
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Horse
-
Cattle
-
Pig
-
Sheep
-
Goat
-
Dog
-
Cat
-
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:
- Available only in Lithuanian
- Available only in Lithuanian
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:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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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