AMOKSIKLAV 500 mg/g + 125 mg/g pulbere pentru administare în apa de băut pentru porci
AMOKSIKLAV 500 mg/g + 125 mg/g pulbere pentru administare în apa de băut pentru porci
Authorised
- Clavulanic acid
- Amoxicillin
Product identification
Medicine name:
AMOKSIKLAV 500 mg/g + 125 mg/g pulbere pentru administare în apa de băut pentru porci
Active substance:
- Clavulanic acid
- Amoxicillin
Target species:
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Clavulanic acid125.00/milligram(s)1.00gram(s)
-
Amoxicillin500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
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:
-
Romania
Available in:
-
Romania
Package description:
- Available only in Romanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Elanco GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Lek Pharmaceuticals d.d.
- Lek Pharmaceuticals d.d.
- PROVET S.A.
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 190008
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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Romanian (PDF)
Published on: 20/03/2025