Veterinary Medicines

Zoletil 50, 125 mg + 125 mg, liofilizatas ir tirpiklis injekciniam tirpalui ruošti šunims ir katėms

Authorised
  • Zolazepam hydrochloride
  • Tiletamine hydrochloride
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Product identification

Medicine name:
Zoletil 50, 125 mg + 125 mg, liofilizatas ir tirpiklis injekciniam tirpalui ruošti šunims ir katėms
Active substance:
  • Zolazepam hydrochloride
  • Tiletamine hydrochloride
Target species:
  • Dog
  • Cat
Route of administration:
  • Intravenous use
  • Intramuscular use

Product details

Active substance and strength:
  • Zolazepam hydrochloride
    125.00
    milligram(s)
    /
    1.00
    Vial
  • Tiletamine hydrochloride
    125.00
    milligram(s)
    /
    1.00
    Vial
Pharmaceutical form:
  • Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Dog
      • Not applicable
        0
        day
  • Intramuscular use
    • Cat
      • Not applicable
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN01AX99
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
  • Valid
Authorised in:
  • Lithuania
Package description:

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:
  • Virbac
Responsible authority:
  • State Food And Veterinary Service
Authorisation number:
  • LT/2/05/1691/001
Date of authorisation status change:

Documents

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Lithuanian (PDF)
Published on: 12/10/2023
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