Haemate Fviii/1 Vwf
Combination product
This product contains more than one active ingredient, so it has no single molecular structure.
Registration
- Applicants
- 1
- Registrations
- 1
Applicants and registrations
| Applicant | Brands | Dosages | Registrations | Schedule | Leaflets |
|---|---|---|---|---|---|
| Gen-eye (Pty) Ltd | Haemate fviii/1 vwf | 500 IU 200 IU | 570351 | Not determined | None |
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Haemate 500 IU fviii/1 200 IU vwf EACH VIAL CONTAINS: HUMAN COAGULATION FACTOR VIII 500,0 IU HUMAN VON WILLEBRAND FACTOR 1 200,0 IU | 500 IU 200 IU | 57035157/30.3/0351 | 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.
Background
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.