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Tulobuterol (Bremax)

Tulobuterol

Abbott Laboratories S.A. (Pty) Ltd

Registration

Applicant
Abbott Laboratories S.A. (Pty) Ltd
Registrations
2

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Bremax tablets

EACH TABLET CONTAINS TULOBUTEROL HYDROCHLORIDE 2,0 mg

TabletsV0265V/10.2/265RegisteredNot determinedNone
Bremax syrup*

EACH 5 ml SYRUP CONTAINS TULOBUTEROL HYDROCHLORIDE 1,0 mg

SyrupV0266V/10.1/266RegisteredNot 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: Tulobuterol

    • when contained in respirator solutions.

    Consolidated Schedules 06 July 2026, line 4364

  • S2: Tulobuterol

    • except when contained in respirator solutions.

    Consolidated Schedules 06 July 2026, line 2749

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.

C12H18ClNO227.73 g/mol

2-(tert-Butylamino)-1-(2-chlorophenyl)ethanol

Drag to rotate. Structure from PubChem CID 5606.

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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