Cartilago comp. "Wala" - Injektionslösung für Tiere
Cartilago comp. "Wala" - Injektionslösung für Tiere
Authorised
- ECHINACEA PALLIDA E PLANTA TOTA FERM 33C DIL. D2 (HAB, VS. 33C)
- ARTICULATIO INTERPHALANGEA BOVIS GL DIL. D16 (HAB, VS. 41B)
- QUARZ DIL. D29 AQUOS.
Product identification
Medicine name:
Cartilago comp. "Wala" - Injektionslösung für Tiere
Active substance:
- ECHINACEA PALLIDA E PLANTA TOTA FERM 33C DIL. D2 (HAB, VS. 33C)
- ARTICULATIO INTERPHALANGEA BOVIS GL DIL. D16 (HAB, VS. 41B)
- QUARZ DIL. D29 AQUOS.
Target species:
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Horse
-
Cat
-
Rabbit
-
Guinea pig
-
Hamster
-
Rat
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
ECHINACEA PALLIDA E PLANTA TOTA FERM 33C DIL. D2 (HAB, VS. 33C)100.00/milligram(s)1.00millilitre(s)
-
ARTICULATIO INTERPHALANGEA BOVIS GL DIL. D16 (HAB, VS. 41B)100.00/milligram(s)1.00millilitre(s)
-
QUARZ DIL. D29 AQUOS.100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0hour
-
-
Dog
-
Goat
-
Meat and offal0day
-
Milk0hour
-
-
Sheep
-
Meat and offal0day
-
Milk0hour
-
-
Horse
-
Meat and offal0day
-
Milk0hour
-
-
Cat
-
Rabbit
-
Meat and offal0day
-
-
Guinea pig
-
Hamster
-
Rat
-
Pig
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0hour
-
Milk0day
-
-
Dog
-
Goat
-
Meat and offal0day
-
Milk0hour
-
-
Sheep
-
Meat and offal0day
-
Milk0hour
-
-
Horse
-
Meat and offal0day
-
Milk0hour
-
-
Cat
-
Rabbit
-
Meat and offal0day
-
-
Guinea pig
-
Hamster
-
Rat
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QV03AX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
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:
- SaluVet GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Wala-Heilmittel GmbH
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-30014
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 12/05/2015
Updated on: 8/01/2025
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: 12/05/2015
Updated on: 8/01/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 12/05/2015
Updated on: 8/01/2025
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