KETOXYME
KETOXYME
Authorised
- Ketoprofen
Product identification
Medicine name:
KETOXYME
Ketoxyme 100 mg/ml oplossing voor gebruik in drinkwater
Active substance:
- Ketoprofen
Target species:
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Ketoprofen100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Pig
-
Meat and offal2day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AE03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- bottle of 1 L
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Andersen S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Labiana Life Sciences S.A.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 114768
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0213/001
Concerned member states:
-
Belgium
-
Netherlands
-
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
This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/01/2022
Summary of Product Characteristics
English (PDF)
Download Published on: 5/04/2023
Package Leaflet
English (PDF)
Download Published on: 5/04/2023
eu-PUAR-ketoxyme-en.pdf
English (PDF)
Download Published on: 5/04/2023
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