AMOXICILLINA TRIIDRATO 80%, 800 mg/g, milteliai naudoti su geriamuoju vandeniu vištoms, kalakutams ir kiaulėms
AMOXICILLINA TRIIDRATO 80%, 800 mg/g, milteliai naudoti su geriamuoju vandeniu vištoms, kalakutams ir kiaulėms
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
AMOXICILLINA TRIIDRATO 80%, 800 mg/g, milteliai naudoti su geriamuoju vandeniu vištoms, kalakutams ir kiaulėms
Active substance:
- Amoxicillin trihydrate
Target species:
-
Chicken
-
Turkey
-
Pig
Route of administration:
-
In drinking water use
-
In-feed use
Product details
Active substance and strength:
-
Amoxicillin trihydrate800.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken
-
Meat1dayNot authorized for use in birds, whose eggs are intended for human consumption.
-
-
Turkey
-
Meat2dayNot authorized for use in birds, whose eggs are intended for human consumption.
-
-
Pig
-
Meat1day
-
-
-
In-feed use
-
Chicken
-
Meat1dayNot authorized for use in birds, whose eggs are intended for human consumption.
-
-
Turkey
-
Meat2dayNot authorized for use in birds, whose eggs are intended for human consumption.
-
-
Pig
-
Meat1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Available in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Chemifarma S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Chemifarma S.p.A.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/10/1938/001-005
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Lithuanian (PDF)
Published on: 2/02/2026