ANTOX 9 max
ANTOX 9 max
Authorised
- Clostridium sordellii, toxoid
- Clostridium tetani, toxoid
- Clostridium chauvoei, toxoid
- Clostridium novyi, strain 754, toxoid
- Clostridium novyi, type B, strain 34, toxoid
- Clostridium septicum, strain 1098, Inactivated
- Clostridium perfringens, type D, strain 98, toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type A, strain 28, toxoid
Product identification
Medicine name:
АНТОКС 9 макс
ANTOX 9 max
Active substance:
- Clostridium sordellii, toxoid
- Clostridium tetani, toxoid
- Clostridium chauvoei, toxoid
- Clostridium novyi, strain 754, toxoid
- Clostridium novyi, type B, strain 34, toxoid
- Clostridium septicum, strain 1098, Inactivated
- Clostridium perfringens, type D, strain 98, toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type A, strain 28, toxoid
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium sordellii, toxoid1.00international unit(s)1.00Dose
-
Clostridium tetani, toxoid1.00international unit(s)1.00Dose
-
Clostridium chauvoei, toxoid5.00billion colony forming units1.00Dose
-
Clostridium novyi, strain 754, toxoid6000.00Decimal potentisation1.00Dose
-
Clostridium novyi, type B, strain 34, toxoid6000.00Decimal potentisation1.00Dose
-
Clostridium septicum, strain 1098, Inactivated5.00billion colony forming units1.00Dose
-
Clostridium perfringens, type D, strain 98, toxoid5.00international unit(s)1.00Dose
-
Clostridium perfringens, type C, beta toxoid10.00international unit(s)1.00Dose
-
Clostridium perfringens, type A, strain 28, toxoid0.50international unit(s)1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Sheep
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
- QI04AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Mintech Co EOOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Mintech Co EOOD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-3086
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.
Bulgarian (PDF)
Published on: 8/06/2022
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 8/06/2022
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