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Straxet

Active ingredient not listed in the SAHPRA register

Every registration of this product has been cancelled.

No structure available

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

Registration

Applicants
1
Registrations
6

Applicants and registrations

ApplicantBrandsDosagesRegistrationsScheduleLeaflets
Pharma Dynamics (Pty) LtdCancelledStraxet18 mg, 25 mg, 40 mg, 60 mg, 80 mg, 100 mg510384.377, 510385.378, 510386.379, 510387.38, 510388.381, 510389.382Not determinedNone

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Straxet 18 MG18 mg510384.37751/1.2/0384.377CancelledNot determinedNone
Straxet 25 MG25 mg510385.37851/1.2/0385.378CancelledNot determinedNone
Straxet 40 MG40 mg510386.37951/1.2/0386.379CancelledNot determinedNone
Straxet 60 MG60 mg510387.3851/1.2/0387.380CancelledNot determinedNone
Straxet 80 MG80 mg510388.38151/1.2/0388.381CancelledNot determinedNone
Straxet 100 MG100 mg510389.38251/1.2/0389.382CancelledNot 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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