Narkamon 100 mg/ml Roztwór do wstrzykiwań
Narkamon 100 mg/ml Roztwór do wstrzykiwań
Authorised
- Ketamine
Product identification
Medicine name:
Narkamon 100 mg/ml Roztwór do wstrzykiwań
Active substance:
- Ketamine
Target species:
-
Dog
-
Horse
-
Cat
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Ketamine115.40/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Dog
-
Horse
-
All relevant tissuesno withdrawal periodProduct not approved for use in horses intended for human consumption. Horses treated with the product must be marked as not intended for human consumption in the animal treatment book and on the identification document (passport) accompanying registered equines.
-
-
Cat
-
-
Intravenous use
-
Dog
-
Horse
-
All relevant tissuesno withdrawal periodProduct not approved for use in horses intended for human consumption. Horses treated with the product must be marked as not intended for human consumption in the animal treatment book and on the identification document (passport) accompanying registered equines.
-
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Available in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Grabikowski-Grabikowska Przedsiebiorstwo Produkcyjno-Handlowo-Uslugowe Inex Sp. j.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2556
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 16/03/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 16/03/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 16/03/2022
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