Narcostop 5 mg/ml, solution for injection for cats and dogs
Narcostop 5 mg/ml, solution for injection for cats and dogs
Authorised
- Atipamezole hydrochloride
Product identification
Medicine name:
Narcostop 5 mg/ml, solution for injection for cats and dogs
NARCOSTOP 5 MG/ML SOLUTION INJECTABLE POUR CHATS ET CHIENS
Active substance:
- Atipamezole hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Atipamezole hydrochloride5.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QV03AB90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- Cardboard box with 5 vials containing 10 ml. Clear glass (type I) vial with bromobutylrubber stopper (type I) containing 10 ml solution for injection.
- Cardboard box with 10 vials containing 10 ml. Clear glass (type I) vial with bromobutylrubber stopper (type I) containing 10 ml solution for injection.
- Cardboard box with 1 vial containing 10 ml. Clear glass (type I) vial with bromobutylrubber stopper (type I) containing 10 ml solution for injection.
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:
- Le Vet. B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Produlab Pharma B.V.
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/3467071 6/2010
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0139/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Finland
-
France
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Luxembourg
-
Poland
-
Portugal
-
Slovakia
-
Spain
-
Sweden
-
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
English (PDF)
Download Published on: 13/06/2022
Summary of Product Characteristics
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in another language below.
French (PDF)
Published on: 11/12/2024
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: 11/12/2024
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