Amoksiklav 500 mg/g + 125 mg/g prašek za dajanje v vodo za pitje za prašiče
Amoksiklav 500 mg/g + 125 mg/g prašek za dajanje v vodo za pitje za prašiče
Authorised
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
Amoksiklav 500 mg/g + 125 mg/g prašek za dajanje v vodo za pitje za prašiče
Active substance:
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate573.88milligram(s)1.00gram(s)
-
Potassium clavulanate148.88milligram(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 offal1dayMeso in organi: 1 dan.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Available in:
-
Slovenia
Package description:
- Available only in Slovenian
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 d.d.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0011/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 22/09/2021
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 22/09/2021
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