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Naproxen (Napgesic)

Naproxen

Cipla Medpro (Pty) Ltd

Registration

Applicant
Cipla Medpro (Pty) Ltd
Registrations
1

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Napgesic

EACH TABLET CONTAINS NAPROXEN 500 mg

Not listed27020227/3.1/0202RegisteredNot 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: Naproxen

    • when contained in preparations intended for application to the skin; (S1, S2)
    • when contained in oral medicinal preparations, intended for human use only containing naproxen as the only active therapeutic substance intended for patients over 16 years of age, for the treatment of mild to moderate pain or fever of inflammatory origin at a maximum dose of 600 milligrams naproxen base (660 milligrams naproxen sodium) in a 24 hour period for a maximum treatment period of 5 days and supplied in a solid dose form as divided doses contained in packs not exceeding the stated maximum treatment peroid. (S1, S2)
    • when intended for the treatment of acute gout attacks, for a maximum treatment period of 5 days in patients over 16 years of age. (S1, S2)

    Consolidated Schedules 06 July 2026, lines 3978 to 3994

  • S2: Naproxen

    • when intended for the treatment of acute gout attacks, for a maximum treatment period of 5 days in patients over 16 years of age; (S3)
    • except when contained in preparations intended for application to the skin;(S1) and
    • except when contained in oral medicinal preparations, intended for human use only containing naproxen as the only active therapeutic substance intended for patients over 16 years of age, for the treatment of mild to moderate pain or fever of inflammatory origin at a maximum dose of 600 milligrams naproxen base (660 milligrams naproxen sodium) in a 24 hour period for a maximum treatment period of 5 days and supplied in a solid dose form as divided doses contained in packs not exceeding the stated maximum treatment period; (S1, S3)
    • except when intended for veterinary use. (S3)

    Consolidated Schedules 06 July 2026, lines 2368 to 2386

  • S1: Naproxen

    • when contained in preparations intended for application to the skin; (S2, S3)
    • when contained in oral medicinal preparations, intended for human use only containing naproxen as the only active therapeutic substance intended for patients over 16 years of age, for the treatment of mild to moderate pain or fever of inflammatory origin at a maximum dose of 600 milligrams naproxen base (660 milligrams naproxen sodium) in a 24 hour period for a maximum treatment period of 5 days and supplied in a solid dose form as divided doses contained in packs not exceeding the stated maximum treatment period; (S2, S3)
    • except when intended for veterinary use. (S3)

    Consolidated Schedules 06 July 2026, lines 866 to 877

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.

C14H14O3230.26 g/mol

(2S)-2-(6-Methoxynaphthalen-2-yl)propanoic acid

Drag to rotate. Structure from PubChem CID 156391.

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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