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Potassium

Sold as Kalimed

Every registration of this product has been cancelled.

No structure available

This product's active ingredient could not be matched to a single known compound.

Background

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Registration

Applicants
1
Registrations
1

Applicants and registrations

ApplicantBrandsDosagesRegistrationsScheduleLeaflets
Swisspharm (Pty) LtdCancelledKalimedinjectionJ0447Not determinedNone

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Kalimed injection*

EACH 10 ml SOLUTION CONTAINS POTASSIUM CHLORIDE EQUIVALENT TO 20 mEq POTASSIUM

InjectionJ0447J/24/447CancelledNot 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: Potassium

    • when intended for intravenous infusion or for injection;
    • except when contained in oral rehydration preparations; (S0)
    • except in oral preparations or mixtures containing more than 20 millimoles (1500mg) of potassium per 24 hours. (S2)

    Consolidated Schedules 06 July 2026, lines 4148 to 4153

  • S2: Potassium

    • in oral preparations or mixtures containing more than 20 millimoles (1500mg) of potassium per 24 hours;
    • except when intended for intravenous infusion or for injection; (S3) and
    • except when contained in oral rehydration preparations. (S0)

    Consolidated Schedules 06 July 2026, lines 2563 to 2569

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.

SAHPRA documents

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

Research articles

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