AMOKSIKLAV 500 mg/g + 125 mg/g prášok na podanie v pitnej vode pre ošípané
AMOKSIKLAV 500 mg/g + 125 mg/g prášok na podanie v pitnej vode pre ošípané
Authorised
- Potassium clavulanate
- Amoxicillin trihydrate
Product identification
Medicine name:
AMOKSIKLAV 500 mg/g + 125 mg/g prášok na podanie v pitnej vode pre ošípané
Active substance:
- Potassium clavulanate
- Amoxicillin trihydrate
Target species:
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Potassium clavulanate148.88/milligram(s)1.00gram(s)
-
Amoxicillin trihydrate573.88/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
In drinking water use
-
Pig
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Package description:
- Available only in Slovak
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lek Pharmaceuticals d.d.
- Lek Pharmaceuticals d.d.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/0651/97-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Slovak (PDF)
Published on: 19/03/2025