Fendov 1250 avec Systamex 1250 mg Intraruminaal hulpmiddel met intermitterende afgifte
Fendov 1250 avec Systamex 1250 mg Intraruminaal hulpmiddel met intermitterende afgifte
Not authorised
- Oxfendazole
Product identification
Medicine name:
Fendov 1250 avec Systamex 1250 mg Intraruminaal hulpmiddel met intermitterende afgifte
Fendov 1250 avec Systamex 1250 mg Dispositif intraruminal à libération séquentielle
Fendov 1250 avec Systamex 1250 mg Intraruminales System mit pulsierender Freigabe
Active substance:
- Oxfendazole
Target species:
-
Cattle
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Oxfendazole1250.00/milligram(s)1.00System
Pharmaceutical form:
-
Pulsatile-release intraruminal device
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal7month
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Fendov 1250 avec Systamex Container with 24 Boluses Pulsatile-release intraruminal device
- Fendov 1250 avec Systamex Container with 12 Boluses Pulsatile-release intraruminal device
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V301061
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
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Package Leaflet
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Labelling
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