ZEEL, injekcinis tirpalas
ZEEL, injekcinis tirpalas
Authorised
- CARTILAGO SUIS D6
- FUNICULUS UMBILICALIS SUIS D6
- EMBRYO SUIS
- PLACENTA SUIS
- SYMPHYTUM OFFICINALE D6
- SOLANUM DULCAMARA D3
- NADIDUM D8
- COENZYM A D8
- SANGUINARIA CANADENSIS D4
- ARNICA MONTANA
- SULFUR D6
- NATRIUM DIETHYLOXALACETICUM D8
- ACIDUM ALPHA-KETOGLUTARICUM D8
- RHUS TOXICODENDRON D2
Product identification
Medicine name:
ZEEL, injekcinis tirpalas
Active substance:
- CARTILAGO SUIS D6
- FUNICULUS UMBILICALIS SUIS D6
- EMBRYO SUIS
- PLACENTA SUIS
- SYMPHYTUM OFFICINALE D6
- SOLANUM DULCAMARA D3
- NADIDUM D8
- COENZYM A D8
- SANGUINARIA CANADENSIS D4
- ARNICA MONTANA
- SULFUR D6
- NATRIUM DIETHYLOXALACETICUM D8
- ACIDUM ALPHA-KETOGLUTARICUM D8
- RHUS TOXICODENDRON D2
Target species:
-
Horse
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
CARTILAGO SUIS D65.00microlitre(s)1.00Ampoule
-
FUNICULUS UMBILICALIS SUIS D65.00microlitre(s)1.00Ampoule
-
EMBRYO SUIS5.00microlitre(s)1.00Ampoule
-
PLACENTA SUIS5.00microlitre(s)1.00Ampoule
-
SYMPHYTUM OFFICINALE D625.00microlitre(s)1.00Ampoule
-
SOLANUM DULCAMARA D325.00microlitre(s)1.00Ampoule
-
NADIDUM D85.00microlitre(s)1.00Ampoule
-
COENZYM A D85.00microlitre(s)1.00Ampoule
-
SANGUINARIA CANADENSIS D47.50microlitre(s)1.00Ampoule
-
ARNICA MONTANA50.00microlitre(s)1.00Ampoule
-
SULFUR D69.00microlitre(s)1.00Ampoule
-
NATRIUM DIETHYLOXALACETICUM D85.00microlitre(s)1.00Ampoule
-
ACIDUM ALPHA-KETOGLUTARICUM D85.00microlitre(s)1.00Ampoule
-
RHUS TOXICODENDRON D225.00microlitre(s)1.00Ampoule
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Horse
-
Dog
-
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/2/03/1539/001-002
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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