Dolutegravir (Tivicay)
Dolutegravir
Glaxosmithkline South Africa (Pty) Limited
Every registration of this product has been cancelled.
Registration
- Applicant
- Glaxosmithkline South Africa (Pty) Limited
- Registrations
- 1
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Tivicay 25 MG Each Tablet Contains: Dolutegravir sodium Equivalent to Dolutegravir 25 mg | 25 mg | 51037151/20.2.8/0371 | 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
S4: Dolutegravir
Consolidated Schedules 06 July 2026, line 6100
S4: Lamivudine
Consolidated Schedules 06 July 2026, line 6850
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.
(3S,7R)-N-[(2,4-Difluorophenyl)methyl]-11-hydroxy-7-methyl-9,12-dioxo-4-oxa-1,8-diazatricyclo[8.4.0.03,8]tetradeca-10,13-diene-13-carboxamide
Drag to rotate. Structure from PubChem CID 54726191.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.