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Fenoprofen (Fenopron, Fenopron-t)

Fenoprofen

Pharmacare limited û woodmead

Every registration of this product has been cancelled.

Registration

Applicant
Pharmacare limited û woodmead
Registrations
2

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Fenopron 300

EACH CAPSULE CONTAINS FENOPROFEN CALCIUM EQUIVALENT TO 300 mg FENOPROFEN

300F0092F/3.2/92CancelledNot determinedNone
Fenopron-t

EACH TABLET CONTAINS FENOPROFEN CALCIUM EQUIVALENT TO FENOPROFEN 600 mg

Not listedH0097H/3.2/97CancelledNot 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

  • S3: Fenoprofen

    • except when intended for the emergency treatment of acute gout attacks, (S2) and
    • when intended for the treatment of post traumatic conditions, for a maximum treatment period of 5 days. (S2)

    Consolidated Schedules 06 July 2026, lines 3569 to 3574

  • S2: Fenoprofen

    • when intended for the emergency treatment of acute gout attacks, and
    • when intended for the treatment of post-traumatic conditions, for a maximum treatment period of 5 days. (S3)

    Consolidated Schedules 06 July 2026, lines 1971 to 1982

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.

C15H14O3242.27 g/mol

2-(3-Phenoxyphenyl)propanoic acid

Drag to rotate. Structure from PubChem CID 3342.

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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