Zolazepam (Zoletil)
Zolazepam
Virbac Rsa (Pty) Ltd
Registration
- Applicant
- Virbac Rsa (Pty) Ltd
- Registrations
- 1
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Zoletil 100 * EACH VIAL CONTAINS TILETAMINE HYDROCHLORIDE EQUIVALENT TO 250 mg TILETAMINE ZOLAZEPAM HYDROCHLORIDE EQUIVALENT TO 250 mg ZOLAZEPAM | 100 | 87/1087/2.1/10 | Registered | Not determined | None |
Regulatory status
This product is still scheduled by law even when this site could not determine which tier it falls under. The label carries the S number in a square border; ask a pharmacist if you need to know its schedule.
Listings for this ingredient that could not be applied to this product
S5: Tiletamine
Consolidated Schedules 06 July 2026, line 9721
S5: Zolazepam
Consolidated Schedules 06 July 2026, line 9775
This is an informational summary of the Medicines and Related Substances Act 101 of 1965 and its 2017 General Regulations. It is not medical advice and not legal advice. Always check the medicine's label, which carries the schedule number inside a square border, or ask a pharmacist if you are unsure.
4-(2-Fluorophenyl)-1,3,8-trimethyl-6H-pyrazolo[5,4-e][1,4]diazepin-7-one
Drag to rotate. Structure from PubChem CID 35775.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.