Huvamox 800 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs
Huvamox 800 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Huvamox 800 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs
HUVAMOX 800 mg/g prášok na použitie v pitnej vode pre kurčatá, morky, kačice a ošípané
Active substance:
- Amoxicillin trihydrate
Target species:
-
Turkey
-
Chicken
-
Duck
-
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
- Turkey
-
Meat and offal5day
-
- Chicken
-
Meat and offal1day
-
- Duck
-
Meat and offal9day
-
- 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:
-
Slovakia
Available in:
-
Slovakia
Package description:
- Zipped 1 kg bag made of low density polyethylene/aluminium/polyethylene terephthalate.
- Zipped 500 g bag made of low density polyethylene/aluminium/polyethylene terephthalate.
- Thermo-sealed 100 g bag made of low density polyethylene/aluminium/polyethylene terephthalate.
- 100 g jar 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:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Huvepharma
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/008/DC/21-S
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0642/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
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
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 8/02/2024
Summary of Product Characteristics
English (PDF)
Download Published on: 11/02/2022
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