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Lisdexamfetamine dimesilate (Vyvanse, Vysera)

Lisdexamfetamine dimesilate

Takeda (Pty) Ltd

Registration

Applicant
Takeda (Pty) Ltd
Registrations
6

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Vyvanse 30

LISDEXAMFETAMINE DIMESILATE 30,0 mg

3048040748/1.6/0407RegisteredNot determinedNone
Vyvanse 50

LISDEXAMFETAMINE DIMESILATE 50,0 mg

5048040848/1.6/0408RegisteredNot determinedNone
Vyvanse 70

LISDEXAMFETAMINE DIMESILATE 70,0 mg

7048040948/1.6/0409RegisteredNot determinedNone
Vysera 30 MG

EACH CAPSULE CONTAINS: LISDEXAMFETAMINE DIMESILATE 30,0 mg

30 mg60079960/1.6/0799RegisteredNot determinedNone
Vysera 50 MG

EACH CAPSULE CONTAINS: LISDEXAMFETAMINE DIMESILATE 50,0 mg

50 mg60080060/1.6/0800RegisteredNot determinedNone
Vysera 70 MG

EACH CAPSULE CONTAINS: LISDEXAMFETAMINE DIMESILATE 70,0 mg

70 mg60080160/1.6/0801RegisteredNot determinedNone

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.

Background

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Research articles

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