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Mefenamic acid (Ponac, Ponac Forte)

Mefenamic acid

Pharmacorp (Pty) Ltd

S3Read from the PI-PIL document and verified

Registration

Applicant
Pharmacorp (Pty) Ltd
Certificate holder
Pharmacorp (Pty) Ltd
Registrations
3
Schedule source
SAHPRA documentation

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Ponac capsules

EACH CAPSULE CONTAINS MEFENAMIC ACID 250 MG

250 mgCapsulesY0157Y/2.7/157Approved 28 September 2023RegisteredS3PIPIL
Ponac forte

EACH TABLET CONTAINS MEFENAMIC ACID 500 MG

500 mgTabletsY0158Y/2.7/158Approved 28 September 2023RegisteredS2PIPIL
Ponac suspension

EACH 5 ML SUSPENSION CONTAINS MEFENAMIC ACID 50 MG

50 mg per 5 mlSuspensionY0192Y/2.7/192Approved 4 May 2023RegisteredS2PIPIL

Regulatory status

Where S3 sits on the scale

Needs a doctor's prescription, dispensed by a pharmacist.

Schedule 3 medicines can only be sold on a prescription from an authorised prescriber, such as a doctor or dentist. A pharmacist dispenses the medicine once they have the written prescription, or a verbal instruction from a prescriber they know. Its price, name, pack size and strength can still be told to the public, as long as nothing links it to what it treats.

Schedule S3, read from the product's PI-PIL leaflet.

Who may supply: A pharmacist dispensing against a written or verbal prescription from an authorised prescriber; a veterinarian, who may also prescribe, compound or dispense it directly; a medical practitioner or dentist, who may prescribe it and may compound or dispense it directly only if licensed under section 22C(1)(a); manufacturers and wholesalers may supply people who may lawfully possess it; and, for animal treatment, a person practising a para-veterinary profession, on a veterinarian's written or verbal instruction.

Consolidated Schedules listings for Mefenamic acid

  • S3: Mefenamic acid

    • when intended for the treatment of post-traumatic conditions, for a maximum period of 5 days; and
    • preparations containing mefenamic acid as the only therapeutic active substance, when intended for human use only in the treatment of primary dysmenorrhoea subject to a maximum daily dose of 500 millligrams mefenamic acid 3 times a day and a maximum treatment period of 3 days. (S2)

    Consolidated Schedules 06 July 2026, lines 3915 to 3921

  • S2: Mefenamic acid

    • when intended for the treatment of post-traumatic conditions, for a maximum treatment period of 5 days; and
    • preparations containing mefenamic acid as the only therapeutically active substance, when intended for human use only in the treatment of primary dysmenorrhoea, subject to a maximum daily dose of 500 millligrams 3 times a day and a maximum treatment period of 3 days; (S3)
    • except when intended for veterinary use. (S3)

    Consolidated Schedules 06 July 2026, lines 2271 to 2280

Pharmacological class: Antipyretics or antipyretic and anti-inflammatory analgesics. (class 2.7)

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.

C15H15NO2241.28 g/mol

2-(2,3-Dimethylanilino)benzoic acid

Drag to rotate. Structure from PubChem CID 4044.

SAHPRA documents

Schedule verified from official documents

Schedule Verification

This medication's schedule (S3) has been verified from official SAHPRA documents with 90% confidence.

These documents are provided by SAHPRA for informational purposes. Always consult with a healthcare professional for medical advice.

Background

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Research articles

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