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Rizatriptan (Rizatriptan Odt Viatris)

Rizatriptan

Viatris South Africa (Pty) Ltd

Registration

Applicant
Viatris South Africa (Pty) Ltd
Registrations
2

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Rizatriptan 5 MG odt viatris

EACH TABLET CONTAINS:RIZATRIPTAN BENZOATE EQUIVALENT TO RIZATRIPTAN 5,0 mg

5 mg46021746/7.3/0217RegisteredNot determinedNone
Rizatriptan 10 MG odt viatris

EACH TABLET CONTAINS:RIZATRIPTAN BENZOATE EQUIVALENT TO RIZATRIPTAN 10,0 mg

10 mg46021846/7.3/0218RegisteredNot 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

  • S4: Rizatriptan

    • except when in oral solid dosage forms providing 5 mg or less and presented as packs of no more than 2 oral solid dosage forms, indicated for the acute relief of migraine attacks, with or without aura, in patients previously diagnosed by a medical practitioner and initiated on treatment with rizatriptan (S2)

    Consolidated Schedules 06 July 2026, lines 7826 to 7828

  • S2: Rizatriptan

    • when in oral solid dosage forms providing 5 mg or less and presented as packs of no more than 2 oral solid dosage forms, indicated for the acute relief of migraine attacks, with or without aura, in patients previously diagnosed by a medical practitioner and initiated on treatment with rizatriptan (S4)

    Consolidated Schedules 06 July 2026, lines 2642 to 2644

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.

C15H19N5269.34 g/mol

N,N-Dimethyl-2-[5-(1,2,4-triazol-1-ylmethyl)-1H-indol-3-yl]ethanamine

Drag to rotate. Structure from PubChem CID 5078.

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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