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Amfexa

Active ingredient not listed in the SAHPRA register

No structure available

The SAHPRA register lists no active ingredient for this product, so there is no compound to show.

Registration

Applicants
1
Registrations
3

Applicants and registrations

ApplicantBrandsDosagesRegistrationsScheduleLeaflets
Adcock ingram limitedAmfexa5 mg, 10 mg, 20 mg520871, 520872, 520873Not determinedNone

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Amfexa 5 MG5 mg52087152/1.2/0871RegisteredNot determinedNone
Amfexa 10 MG10 mg52087252/1.2/0872RegisteredNot determinedNone
Amfexa 20 MG20 mg52087352/1.2/0873RegisteredNot 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.

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.

Background

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SAHPRA documents

SAHPRA has not published a professional information or patient information leaflet for this product.

Research articles

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