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Telazol
Tiletamine/Zolazepam · Zoetis
1 form: solution. In force in Georgia: 1 of 1 (veterinary register).
Forms and doses1 of 1 in force in Georgia
The dose from the product's label, by species and weight. Check the label of the pack you use.
| Form | Species | Dose | Frequency | Georgia | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100 mg/ml, Solution · Cat | Cat | Anaesthesia for Dentistry, Abscesses or Foreign Bodies · Intramuscular: 0.097–0.119 ml/kgAnaesthesia for Minor Surgery or Short Anaesthesia · Intramuscular: 0.106–0.125 ml/kgAnaesthesia for Ovariohysterectomy or Onychectomy · Intramuscular: 0.143–0.158 ml/kg | - |
Georgia
Yes, veterinary
Veterinary (National Food Agency)
In the register: თელაზოლი®
Verified on: 22 Oct 2026 |
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| 100 mg/ml, Solution · Dog | Dog | Anaesthesia for Tests and Procedures Causing Little Pain · Intramuscular: 0.066–0.099 ml/kgAnaesthesia for Minor Surgery or Short Anaesthesia · Intramuscular: 0.099–0.132 ml/kgIntravenous Induction before Inhalant Maintenance · Intravenous: 0.022–0.044 ml/kg | - |
Georgia
Yes, veterinary
Veterinary (National Food Agency)
In the register: თელაზოლი®
Verified on: 22 Oct 2026 |
||||||||||||||||
Details: pack, label wording, sources, registrationtiletamine 250 mg + zolazepam 250 mg, powder for solution for injection for dogs and cats Composition / strength
Tiletamine/Zolazepam100 mg/ml
Formulation Type Solution Administration route Intramuscular, Intravenous Manufacturer Zoetis · United States Registration
Georgia
Yes, veterinary
Veterinary (National Food Agency)
In the register: თელაზოლი®
Verified on: 22 Oct 2026 Verified on: 22 Oct 2026 Verified on: 22 Oct 2026 Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 18 Oct 2026
Source:
FDA 2022
Official product label (SPC), FDA, US Approved by the US Food and Drug Administration (FDA) as part of the product's authorisation. It applies to that product as authorised there. US Food and Drug Administration (DailyMed), 2022
Source:
FDA 2022
Official product label (SPC), FDA, US Approved by the US Food and Drug Administration (FDA) as part of the product's authorisation. It applies to that product as authorised there. US Food and Drug Administration (DailyMed), 2022 | ||||||||||||||||||||
Known Contraindications
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Critical
Do not use in animals hypersensitive to tiletamine, zolazepam or the excipients (benzyl alcohol, lactose).
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Critical
Do not use in animals with severe heart disease.
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Critical
Do not use in animals with severe respiratory disease.
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Critical
Do not use in animals with renal insufficiency.
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Critical
Do not use in animals with hepatic insufficiency.
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Critical
Do not use in severe hypertension.
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Critical
Do not use in pregnant bitches and queens or for caesarean section: it crosses the placenta and can cause fatal respiratory depression in newborns.
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Critical
Do not use tiletamine/zolazepam in dogs or cats with pancreatic disease.Sources: Zoletil 100 UK SPC · FDA
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Warning
Safety in lactation has not been established; use only after a benefit-risk assessment.
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Caution
Do not use in severe hypertension, head trauma or intracranial tumours, pancreatic insufficiency, for caesarean section, or in rabbits. Do not give chloramphenicol before or during the anaesthetic; acepromazine premedication deepens cardiorespiratory depression and hypothermia; reduce the dose with other premedicants. Eyes stay open (protect the cornea); reflexes are kept; keep warm; redosing prolongs and worsens recovery. Overdose signs from 20 mg/kg; no antidote (doxapram may help).
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Caution
Not recommended in very young animals: the solvent contains benzyl alcohol.
Professional reference for veterinary professionals. Not advertising and not a substitute for the product label/SPC.
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This reference is still growing. Missing a product? Let us know. · Report an error or request an addition · Updated: 22 Oct 2026