Doxorubicin Hexal
Active ingredient not listed in the SAHPRA register
Sandoz South Africa (Pty) Ltd
Every registration of this product has been cancelled.
Registration
- Applicant
- Sandoz South Africa (Pty) Ltd
- Registrations
- 2
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Doxorubicin hexal 10 mg/5 ML Each 5,0ml Solution Contains: Doxorubicin Hydrochloride | 10 mg/5 ml | 37002837/26/0028 | Cancelled | Not determined | None |
| Doxorubicin hexal 50 mg/25 ML Each 25 ml Solution contains: Doxorubicin Hydrochloride | 50 mg/25 ml | 37002937/26/0029 | 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.
No structure available
The SAHPRA register lists no active ingredient for this product, so there is no compound to show.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.