Emicizumab (Hemlibra)
Emicizumab
Roche Products (Pty) Ltd
Registration
- Applicant
- Roche Products (Pty) Ltd
- Registrations
- 4
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Hemlibra 30 mg/ml EACH 1,0 ml CONTAINS EMICIZUMAB 30,0 mg | 30 mg/ml | 53007153/30.1/0071 | Registered | Not determined | None |
| Hemlibra 60 mg/0,4 ML EACH 0,4 ml CONTAINS EMICIZUMAB 60,0 mg | 60 mg/0,4 ml | 53007253/30.1/0072 | Registered | Not determined | None |
| Hemlibra 105 mg/0,7 ML EACH 0,7 ml CONTAINS EMICIZUMAB 105,0 mg | 105 mg/0,7 ml | 53007353/30.1/0073 | Registered | Not determined | None |
| Hemlibra 150 mg/ ML EACH 1,0 ml CONTAINS EMICIZUMAB 150,0 mg | 150 mg/ ml | 53007453/30.1/0074 | Registered | 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
This product's active ingredient could not be matched to a single known compound.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.