Ketiva 150 mg/ml solution for injection for cattle, pigs and horses
Ketiva 150 mg/ml solution for injection for cattle, pigs and horses
Authorised
- Ketoprofen
Product identification
Medicine name:
Ketiva 150 mg/ml solution for injection for cattle, pigs and horses
Active substance:
- Ketoprofen
Target species:
-
Pig
-
Cattle
-
Horse
Route of administration:
-
Solution for injection
Product details
Active substance and strength:
-
Ketoprofen150.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Solution for injection
-
Pig
-
Meat and offal3day
-
-
Cattle
-
Meat and offal2day
-
Milk0day
-
-
Horse
-
Milkno withdrawal periodNot authorised for use in mares producing milk for human consumption.
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AE03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Amber glass vial type II, closed with a bromobutyl rubber stopper and aluminium pull off cap or aluminium/plastic flip off cap.
- Amber glass vial type II, closed with a bromobutyl rubber stopper and aluminium pull off cap or aluminium/plastic flip off cap.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application – change in therapeutic indication(s) (Article 19(1)(a) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetviva Richter GmbH
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/1364935 9/2026
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0149/001/DC
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Norway
-
Poland
-
Romania
-
Slovakia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
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.
French (PDF)
Published on: 7/04/2026
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 7/04/2026
Combined File of all Documents
English (PDF)
Download Published on: 2/04/2026