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C28H37ClO7521.00 g/mol

[2-[(8S,9R,10S,11S,13S,14S,16S,17R)-9-Chloro-11-hydroxy-10,13,16-trimethyl-3-oxo-17-propanoyloxy-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] propanoate

Drag to rotate; arrow keys step through the atoms. Structure from PubChem CID 21700.

Registration

Applicants
1
Registrations
2

Applicants and registrations

ApplicantBrandsDosagesRegistrationsScheduleLeaflets
Cipla Medpro (Pty) LtdCertificate held by Cipla Medpro (Pty) Ltd.1 of 2 cancelledBeclate aquanase50 µg, 100300079, 340093Not determinedPIPIL

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Beclate aquanase

EACH METERED DOSE CONTAINS BECLOMETHASONE DIPROPIONATE 50,0 mcg

50 µgNasal spray30007930/21.5.1/0079Approved 5 January 2022RegisteredNot determinedPIPIL
Beclate aquanase-100

EACH METERED ACTUATION CONTAINS BECLOMETHASONE DIPROPIONATE 100,0 ug

10034009334/21.5.1/0093CancelledNot determinedPIPIL

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: Beclomethasone dipropionate

    • except when intended for inhalation or nasal administration.

    Consolidated Schedules 06 July 2026, line 5441

  • S3: Beclomethasone dipropionate

    • when intended for inhalation or nasal administration, except when intended for nasal administration as an aqueous spray, other than by pressurised aerosol, and indicated for the treatment of the symptoms of seasonal allergic rhinitis (hay fever) in adults and children over 12 years of age, subject to
    • a maximum dose of 100 micrograms per nostril and a maximum daily dose of 200 micrograms of per nostril and
    • a maximum pack size of 200 doses. (S2, S4)

    Consolidated Schedules 06 July 2026, lines 3170 to 3177

  • S2: Beclomethasone dipropionate

    • when intended for nasal administration as an aqueous spray, other than by pressurised aerosol, and indicated for the treatment of the symptoms of seasonal allergic rhinitis (hay fever) in adults and children over 12 years of age, subject to
    • a maximum dose of 100 micrograms per nostril and a maximum daily dose of 200 micrograms of per nostril and
    • a maximum pack size of 200 doses. (S3, S4)

    Consolidated Schedules 06 July 2026, lines 1647 to 1654

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

These documents come from SAHPRA's PI-PIL repository unless the line under a document says otherwise. Always consult with a healthcare professional for medical advice.

Research articles

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