Zoletil 50 Vet. pulver og solvens til injektionsvæske, opløsning 25 + 25 mg/ml
Zoletil 50 Vet. pulver og solvens til injektionsvæske, opløsning 25 + 25 mg/ml
Authorised
- Tiletamine hydrochloride
- Zolazepam hydrochloride
Product identification
Medicine name:
Zoletil 50 Vet. 25 + 25 mg/ml pulver og solvens til injektionsvæske, opløsning
Zoletil 50 Vet. pulver og solvens til injektionsvæske, opløsning 25 + 25 mg/ml
Active substance:
- Tiletamine hydrochloride
- Zolazepam hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Tiletamine hydrochloride145.50milligram(s)1.00Vial
-
Zolazepam hydrochloride141.00milligram(s)1.00Vial
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Dog
- Cat
-
Intravenous use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- VIRBAC
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 14169
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
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Danish (, PULVER OG SOLVENS TIL INJEKTIONSVÆSKE, OPLØSNING)
Published on: 29/06/2023
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