Aciclovir (Apo-acyclovir)
Aciclovir
Apotex SA (Pty) Ltd
Every registration of this product has been cancelled.
Registration
- Applicant
- Apotex SA (Pty) Ltd
- Registrations
- 2
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Apo-acyclovir 200 MG EACH TABLET CONTAINS ACICLOVIR 200,0 mg | 200 mg | 31042831/20.2.8/0428 | Cancelled | Not determined | None |
| Apo-acyclovir 800 MG EACH TABLET CONTAINS ACICLOVIR 800,0 MG | 800 mg | 31042931/20.2.8/0429 | 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.
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.
2-Amino-9-(2-hydroxyethoxymethyl)-1H-purin-6-one
Drag to rotate. Structure from PubChem CID 135398513.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.