Narcostart (Sedastart) 1 mg/ml solution for injection for cats and dogs
  • Medetomidīna hidrohlorīds
  • Valid
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Product identification

Medicine name:
Narcostart (Sedastart) 1 mg/ml solution for injection for cats and dogs
Narcostart 1 mg/ml Injektionslösung für Hund und Katze
Active substance and strength:
  • Medetomidīna hidrohlorīds
    1.00
    milligram(s)
    /
    1.00
    millilitre(s)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN05CM91
Authorisation number:
  • 8-00867
Product identification number:
  • 40680b5a-e115-41b5-8bc2-fd5d524073f3
Permanent identification number:
  • 600000037128

Product details

Legal status of supply:
This information is not available for this product.
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:
  • Austria
Responsible authority:
  • Austrian Agency For Health And Food Safety Limited
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
  • 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

Package Leaflet (PDF)
First published:
Last updated:
Summary of Product Characteristics (PDF)
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Labelling (PDF)
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Combined File of all Documents (PDF)
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