Awazom 800 mg/g powder for use in drinking water for chickens, ducks and turkeys
Awazom 800 mg/g powder for use in drinking water for chickens, ducks and turkeys
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Awazom 800 mg/g prašek za dajanje v vodo za pitje za kokoši, race in purane
Awazom 800 mg/g powder for use in drinking water for chickens, ducks and turkeys
Active substance:
- Amoxicillin trihydrate
Target species:
-
Chicken
-
Duck
-
Turkey
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate800.00/milligram(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 offal1dayNi za uporabo pri pticah, ki proizvajajo jajca za prehrano ljudi. Ne uporabite v obdobju 3 tednov pred začetkom obdobja nesnosti.
-
-
Duck
-
Meat and offal9dayNi za uporabo pri pticah, ki proizvajajo jajca za prehrano ljudi. Ne uporabite v obdobju 3 tednov pred začetkom obdobja nesnosti.
-
-
Turkey
-
Meat and offal5dayNi za uporabo pri pticah, ki proizvajajo jajca za prehrano ljudi. Ne uporabite v obdobju 3 tednov pred začetkom obdobja nesnosti.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Available in:
-
Slovenia
Package description:
- Thermosealed bags of PET/Al/PE containing 1000 g powder.
- Thermosealed bags of PET/Al/PE containing 500 g powder.
- Thermosealed bags of PET/Al/PE containing 250 g powder.
- Thermosealed bags of PET/Al/PE containing 100 g powder.
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:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- DC/V/0660/001
Date of authorisation status change:
Reference member state:
-
Slovenia
Procedure number:
- SI/V/0002/001
Concerned member states:
-
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
English (PDF)
Download Published on: 29/03/2024
Summary of Product Characteristics
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Slovenian (PDF)
Published on: 29/03/2024
Package Leaflet
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in another language below.
Slovenian (PDF)
Published on: 29/03/2024
Labelling
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in another language below.
Slovenian (PDF)
Published on: 29/03/2024