Miloxan - Injektionssuspension für Rinder, Schafe und Ziegen
Miloxan - Injektionssuspension für Rinder, Schafe und Ziegen
Authorised
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- CLOSTRIDIUM TETANI
- Clostridium chauvoei, Inactivated
- Clostridium sordellii, toxoid
Product identification
Medicine name:
Miloxan - Injektionssuspension für Rinder, Schafe und Ziegen
Active substance:
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- CLOSTRIDIUM TETANI
- Clostridium chauvoei, Inactivated
- Clostridium sordellii, toxoid
Target species:
-
Cattle
-
Goat
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium perfringens, type B and C, beta toxoid10.00international unit(s)2.00millilitre(s)
-
Clostridium perfringens, type D, epsilon toxoid5.00international unit(s)2.00millilitre(s)
-
Clostridium septicum, toxoid2.50international unit(s)2.00millilitre(s)
-
Clostridium novyi, toxoid3.50international unit(s)2.00millilitre(s)
-
CLOSTRIDIUM TETANI2.50international unit(s)2.00millilitre(s)
-
Clostridium chauvoei, Inactivated90.00percentage protection2.00millilitre(s)
-
Clostridium sordellii, toxoid90.00percentage protection2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal0day
-
Milk0hour
-
- Goat
-
Meat and offal0day
-
Milk0hour
-
- Sheep
-
Meat and offal0day
-
Milk0hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
- QI03AB
- QI04AB01
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:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-20126
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: 30/06/2020
Updated on: 11/09/2024
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: 2/09/2020
Updated on: 11/09/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 4/05/2020
Updated on: 11/09/2024
How useful was this page?: