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Cyproheptadine hydrochloride cyproheptadine (Cipla-actin)

Cyproheptadine hydrochloride cyproheptadine

Cipla Medpro (Pty) Ltd

Registration

Applicant
Cipla Medpro (Pty) Ltd
Registrations
1

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Cipla-actin

EACH TABLET CONTAINS CYPROHEPTADINE HYDROCHLORIDE CYPROHEPTADINE 4,0 mg

Not listed36007236/5.7.1/0072RegisteredNot 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

  • S5: Cyproheptadine

    • except when indicated for allergic rhinitis or antipruritic use.

    Consolidated Schedules 06 July 2026, line 9349

  • S2: Cyproheptadine

    • when indicated for allergic rhinitis or antipruritic use.

    Consolidated Schedules 06 July 2026, line 1789

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.

Combination product

This product contains more than one active ingredient, so it has no single molecular structure.

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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