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C5H9NO3S163.20 g/mol

(2R)-2-Acetamido-3-sulfanylpropanoic acid

Drag to rotate; arrow keys step through the atoms. Structure from PubChem CID 12035.

Registration

Applicants
1
Registrations
2

Applicants and registrations

ApplicantBrandsDosagesRegistrationsScheduleLeaflets
Aurogen South Africa (Pty) LtdRocylteine200 mg, 600 mg560143.139, 560144.140Not determinedNone

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Rocylteine 200 MG

EACH TABLET CONTAINS ACETYLCYSTEINE 200,0 mg

200 mg560143.13956/10.3/0143.139RegisteredNot determinedNone
Rocylteine 600 MG

EACH TABLET CONTAINS ACETYLCYSTEINE 600,0 mg

600 mg560144.14056/10.3/0144.140RegisteredNot 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: Acetylcysteine

    • when intended for injection or for the management of paracetamol overdosage;
    • except when used as a mucolytic in acute respiratory conditions for a maximum treatment period of 14 days. (S1)

    Consolidated Schedules 06 July 2026, lines 3109 to 3114

  • S1: Acetylcysteine

    • when used as a mucolytic in acute respiratory conditions for a maximum treatment period of 14 days;
    • except when intended for injection or for the management of paracetamol overdosage. (S3)

    Consolidated Schedules 06 July 2026, lines 102 to 106

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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