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Quinine (Quinine Dihydrochloride Fresenius)

Quinine

Fresenius Kabi Manufacturing SA (Pty) Ltd

Every registration of this product has been cancelled.

Registration

Applicant
Fresenius Kabi Manufacturing SA (Pty) Ltd
Registrations
1

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Quinine dihydrochloride 300 mg/1 ML fresenius

EACH 1 ml SOLUTION CONTAINS QUININE DIHYDROCHLORIDE 300 mg

300 mg/1 ml31026131/12/0261CancelledNot 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

  • S4: Quinine

    • except preparations and mixures containing not more than 1 percent.

    Consolidated Schedules 06 July 2026, line 7695

  • S2: Quinine

    • preparations and mixtures containing not more than 1 percent thereof.

    Consolidated Schedules 06 July 2026, line 2617

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.

No structure available

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

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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