ZOLETIL 100 (50 mg/mL + 50 mg/mL)
ZOLETIL 100 (50 mg/mL + 50 mg/mL)
Authorised
- Tiletamine hydrochloride
- Zolazepam hydrochloride
Product identification
Medicine name:
ZOLETIL 100 (50 mg/mL + 50 mg/mL)
Active substance:
- Tiletamine hydrochloride
- Zolazepam hydrochloride
Target species:
-
Cat
-
Dog
Route of administration:
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Tiletamine hydrochloride250.00/milligram(s)1.00Vial
-
Zolazepam hydrochloride250.00/milligram(s)1.00Vial
Pharmaceutical form:
-
Powder and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intravenous use
- Cat
- Dog
-
Intramuscular use
- Cat
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Croatia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Valdepharm
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/21-01/76
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.
Croatian (PDF)
Published on: 21/06/2023
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