Narcostart (Sedastart) 1 mg/ml solution for injection for cats and dogs
- Medetomidīna hidrohlorīds
-
Valid
Product identification
Medicine name:
Narcostart (Sedastart) 1 mg/ml solution for injection for cats and dogs
Narcostart 1 mg/ml Oplossing voor injectie
Narcostart 1 mg/ml Solution injectable
Narcostart 1 mg/ml Injektionslösung
Active substance and strength:
-
Medetomidīna hidrohlorīds
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN05CM91
Authorisation number:
- BE-V368611
Product identification number:
- 40680b5a-e115-41b5-8bc2-fd5d524073f3
Permanent identification number:
- 600000037129
Product details
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Dog
- Cat
-
Intravenous use
- Dog
- Cat
Availability
Package description:
- 1 x 1 glass vial with 10 ml. Glass (type I) vials closed with bromobutyl rubber closures secured with aluminium crimp caps.
- 5 x 1 glass vial with 10 ml. Glass (type I) vials closed with bromobutyl rubber closures secured with aluminium crimp caps.
Manufacturing sites for batch release:
This information is not available for this product.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.
Authorisation details
Authorisation status:
-
Valid
Authorisation procedure type:
-
Marketing Authorisation
Procedure number:
- NL/V/0138/001
Date of authorisation status change:
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Authorisation country:
-
Belgium
Responsible authority:
- Federal Agency For Medicines And Health Products
Marketing authorisation holder:
- Le Vet. B.V.
Marketing authorisation issued:
Reference member state:
-
Netherlands
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Finland
-
France
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
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Luxembourg
-
Poland
-
Portugal
-
Slovakia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.
Additional information
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Package Leaflet
(PDF)
First published:
Last updated:
Package Leaflet
(PDF)
First published:
Last updated:
Package Leaflet
(PDF)
First published:
Last updated:
First published:
Last updated:
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