Febrisept ReVet RV11 - Injektionslösung für Tiere
Febrisept ReVet RV11 - Injektionslösung für Tiere
Authorised
- Atropa bella-donna C6
- HEPAR SULFURIS C12
- LACHESIS C9
- PHYTOLACCA AMERICANA C6
- PYROGENIUM C12
Product identification
Medicine name:
Febrisept ReVet RV11 - Injektionslösung für Tiere
Active substance:
- Atropa bella-donna C6
- HEPAR SULFURIS C12
- LACHESIS C9
- PHYTOLACCA AMERICANA C6
- PYROGENIUM C12
Target species:
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Horse
-
Cat
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Atropa bella-donna C60.40gram(s)2.00millilitre(s)
-
HEPAR SULFURIS C120.40gram(s)2.00millilitre(s)
-
LACHESIS C90.40gram(s)2.00millilitre(s)
-
PHYTOLACCA AMERICANA C60.40gram(s)2.00millilitre(s)
-
PYROGENIUM C120.40gram(s)2.00millilitre(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
-
Pig
-
Meat and offal0day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal0day
-
Milk0hour
-
-
Dog
-
Goat
-
Meat and offal0day
-
Milk0hour
-
-
Sheep
-
Meat and offal0day
-
Milk0hour
-
-
Horse
-
Meat and offal0day
-
Milk0hour
-
-
Cat
-
Pig
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0hour
-
-
Dog
-
Goat
-
Meat and offal0day
-
Milk0hour
-
-
Sheep
-
Meat and offal0day
-
Milk0hour
-
-
Horse
-
Meat and offal0day
-
Milk0hour
-
-
Cat
-
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:
- Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Pharmazeutische Fabrik Dr. Reckeweg & Co. GmbH
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-30016
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: 23/07/2014
Updated on: 9/07/2024
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: 23/07/2014
Updated on: 9/07/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 7/08/2014
Updated on: 9/07/2024
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