Cyclizine (Aculoid)
Cyclizine
Teva Pharmaceuticals (Pty) Ltd
Every registration of this product has been cancelled.
Registration
- Applicant
- Teva Pharmaceuticals (Pty) Ltd
- Registrations
- 2
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Aculoid syrup EACH 5 ml SOLUTION CONTAINS CYCLIZINE HYDROCHLORIDE 12,5 mg | Syrup | X0005X/5.7/5 | Cancelled | Not determined | None |
| Aculoid tablets EACH TABLET CONTAINS CYCLIZINE HYDROCHLORIDE 50 mg | Tablets | Z0228Z/5.7.2/228 | Cancelled | 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
S2: Cyclizine
Consolidated Schedules 06 July 2026, line 1785
2 of 3 approved products with this ingredient carry S6 on their leaflet.
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.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.