Zoletil, 100, Prášek a rozpouštědlo pro injekční roztok
Zoletil, 100, Prášek a rozpouštědlo pro injekční roztok
Authorised
- Tiletamine
- Zolazepam
Product identification
Medicine name:
Zoletil, 100, Prášek a rozpouštědlo pro injekční roztok
Active substance:
- Tiletamine
- Zolazepam
Target species:
-
Dog
-
Cat
Route of administration:
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Tiletamine50.00/milligram(s)1.00millilitre(s)
-
Zolazepam50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Powder and solvent for solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- Available only in Czech
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
- Valdepharm
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/099/98-C
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.
Czech (PDF)
Published on: 10/11/2025
Labelling
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in another language below.
Czech (PDF)
Published on: 10/11/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 10/11/2025