Promethazine (Phenergan)
Promethazine
Sanofi-aventis South Africa (Pty) Ltd
Every registration of this product has been cancelled.
Registration
- Applicant
- Sanofi-aventis South Africa (Pty) Ltd
- Certificate holder
- Sanofi-aventis South Africa (Pty) Ltd.
- Registrations
- 2
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Phenergan 10 TABLET PROMETHAZINE HYDROCHLORIDE A 10 MG | 10Film-coated tablets. | C0855Approved 6 November 2023 | Cancelled | Not determined | PIPIL |
| Phenergan 25 MG / ML EACH 1,0 ml CONTAINS PROMETHAZINE HYDROCHLORIDE A 25,0 mg | 25 mg / ml | C0857 | 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: Promethazine
- when intended for use as an antihistamine, and
- when intended for application to the skin, and
- when intended specifically for the treatment of travel sickness. (S5)
Consolidated Schedules 06 July 2026, lines 2586 to 2592
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.
N,N-Dimethyl-1-phenothiazin-10-ylpropan-2-amine
Drag to rotate. Structure from PubChem CID 4927.
SAHPRA documents
These documents are provided by SAHPRA for informational purposes. Always consult with a healthcare professional for medical advice.