Suramox 5 % Premix 50 mg/g Premix voor gemedicineerd voer
Suramox 5 % Premix 50 mg/g Premix voor gemedicineerd voer
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Suramox 5 % Premix 50 mg/g Premix voor gemedicineerd voer
Suramox 5 % Premix 50 mg/g Prémélange médicamenteux
Suramox 5 % Premix 50 mg/g Arzneimittel-Vormischung zur Herstellung von Fütterungsarzneimitteln
Active substance:
- Amoxicillin trihydrate
Target species:
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate57.40/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Premix for medicated feeding stuff
Withdrawal period by route of administration:
-
Oral use
-
Pig
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Suramox 5 % Premix 50 mg/g Premix for medicated feeding stuff Bag 50 kg
- Suramox 5 % Premix 50 mg/g Premix for medicated feeding stuff Bag 25 kg
- Suramox 5 % Premix 50 mg/g Premix for medicated feeding stuff Bag 20 kg
- Suramox 5 % Premix 50 mg/g Premix for medicated feeding stuff Bag 8 kg
- Suramox 5 % Premix 50 mg/g Premix for medicated feeding stuff Bag 6 kg
- Suramox 5 % Premix 50 mg/g Premix for medicated feeding stuff Jar 1kg
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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
- FC France S.A.S.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V375566
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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