NARKAMON 100 MG/ML SOLUTION INJECTABLE
NARKAMON 100 MG/ML SOLUTION INJECTABLE
Authorised
- Ketamine hydrochloride
Product identification
Medicine name:
NARKAMON 100 MG/ML SOLUTION INJECTABLE
Active substance:
- Ketamine hydrochloride
Target species:
-
Dog
-
Cat
-
Donkey
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Ketamine hydrochloride115.34/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Donkey
-
Meat and offal1day
-
Milk24hour
-
-
Horse
-
Meat and offal1day
-
Milk24hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Osalia
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/7340298 3/2022
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.
French (PDF)
Published on: 6/02/2026
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: 6/02/2026
fr-puar-600000098089-np-rpe705-fr.pdf
French (PDF)
Download Published on: 7/01/2026