Amoxy trihydraat 574 mg/g Poeder voor gebruik in drinkwater
Amoxy trihydraat 574 mg/g Poeder voor gebruik in drinkwater
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Amoxy trihydraat 574 mg/g Poeder voor gebruik in drinkwater
Amoxy trihydraat 574 mg/g Poudre pour administration dans l’eau de boisson
Amoxy trihydraat 574 mg/g Pulver zum Eingeben über das Trinkwasser
Active substance:
- Amoxicillin trihydrate
Target species:
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate574.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Pig
-
All relevant tissuesno withdrawal periodFrench:Viande et abats : 2 jours. ; Dutch:(Orgaan)vlees: 2 dagen.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Amoxy trihydraat 2 kg Bag Powder for use in drinking water
- Amoxy trihydraat 1 kg Bag Powder for use in drinking water
- Amoxy trihydraat 750 g Bag Powder for use in drinking water
- Amoxy trihydraat 500 g Bag Powder for use in drinking water
- Amoxy trihydraat 100 g Bag Powder for use in drinking water
- Amoxy trihydraat 75 g Bag Powder for use in drinking water
- Amoxy trihydraat 1 kg Jar Powder for use in drinking water
- Amoxy trihydraat 500 g Jar Powder for use in drinking water
- Amoxy trihydraat 250 g Jar Powder for use in drinking water
- Amoxy trihydraat 100 g Jar Powder for use in drinking water
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:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- V.M.D.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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