Huvacillin 800 mg/g Powder for use in drinking water for chickens and pigs
Huvacillin 800 mg/g Powder for use in drinking water for chickens and pigs
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Huvacillin 800 mg/g Powder for use in drinking water for chickens and pigs
Huvacillin 800 mg/g Poeder voor gebruik in drinkwater
Huvacillin 800 mg/g Poudre pour administration dans l’eau de boisson
Huvacillin 800 mg/g Pulver zum Eingeben über das Trinkwasser
Active substance:
- Amoxicillin trihydrate
Target species:
-
Chicken
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate800.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
Meat and offal1day
-
- Pig
-
Meat and offal2day
-
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:
- Zipped bag of 1kg made of low density polyethylene/aluminium/polyethylene terephthalate.
- Zipped bag of 500g made of low density polyethylene/aluminium/polyethylene terephthalate.
- thermo-sealed sachet of 100g made of low density polyethylene/aluminium/polyethylene terephthalate
- Jar of 100g made of high density polyethylene closed with a seal made of low density polyethylene/ polyethylene terephthalate/aluminium and a screw cap made of polypropylene
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Huvepharma
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0365/001/DC
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
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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