Lisdexamfetamine dimesilate (Vyfocis)
Lisdexamfetamine dimesilate
Cipla Medpro (Pty) Ltd
Registration
- Applicant
- Cipla Medpro (Pty) Ltd
- Registrations
- 3
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Vyfocis 30 EACH CAPSULE CONTAINS: LISDEXAMFETAMINE DIMESILATE 30,0 mg | 30 | 56123856/1.6/1238 | Registered | Not determined | None |
| Vyfocis 50 EACH CAPSULE CONTAINS: LISDEXAMFETAMINE DIMESILATE 50,0 mg | 50 | 56124056/1.6/1240 | Registered | Not determined | None |
| Vyfocis 70 EACH CAPSULE CONTAINS: LISDEXAMFETAMINE DIMESILATE 70,0 mg | 70 | 56124256/1.6/1242 | 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.
Listings for this ingredient that could not be applied to this product
S7: Lisdexamfetamine
- except in medicines registered in terms of the Act and intended for the treatment of Attention-Deficit Hyperactivity Disorder. (S6)
Consolidated Schedules 06 July 2026, lines 10751 to 10752
S6: Lisdexamfetamine
- in medicines registered in terms of the Act and intended for the treatment of Attention-Deficit Hyperactivity Disorder. (S7)
Consolidated Schedules 06 July 2026, lines 10289 to 10290
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.