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zameds

Glycopyrronium, indacaterol, mometasone furoate

Sold as Enerzair breezhaler, Zimbus breezhaler

Combination product

This product contains more than one active ingredient, so it has no single molecular structure.

Background

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Registration

Applicants
1
Registrations
4

Applicants and registrations

ApplicantBrandsDosagesRegistrationsScheduleLeaflets
Novartis South Africa (Pty) LtdEnerzair breezhaler, Zimbus breezhaler150/50/80, 150/50/160540873, 540874, 540875.873, 540876.874Not determinedNone

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Enerzair breezhaler 150/50/80

EACH CAPSULE CONTAINS GLYCOPYRRONIUM BROMIDE EQUIVALENT TO GLYCOPYRRONIUM 50,0 ug INDACATEROL ACETATE EQUIVALENT TO INDACATEROL 150,0 ug MOMETASONE FUROATE 80,0 ug

150/50/8054087354/10.2.1/0873RegisteredNot determinedNone
Enerzair breezhaler 150/50/160

EACH CAPSULE CONTAINS GLYCOPYRRONIUM BROMIDE EQUIVALENT TO GLYCOPYRRONIUM 50,0 ug INDACATEROL ACETATE EQUIVALENT TO INDACATEROL 150,0 ug MOMETASONE FUROATE 160,0 ug

150/50/16054087454/10.2.1/0874RegisteredNot determinedNone
Zimbus breezhaler 150/50/80

EACH CAPSULE CONTAINS GLYCOPYRRONIUM BROMIDE EQUIVALENT TO GLYCOPYRRONIUM 50,0 ug INDACATEROL ACETATE EQUIVALENT TO INDACATEROL 150,0 ug MOMETASONE FUROATE 80,0 ug

150/50/80540875.87354/10.2.1/0875.873RegisteredNot determinedNone
Zimbus breezhaler 150/50/160

EACH CAPSULE CONTAINS GLYCOPYRRONIUM BROMIDE EQUIVALENT TO GLYCOPYRRONIUM 50,0 ug INDACATEROL ACETATE EQUIVALENT TO INDACATEROL 150,0 ug MOMETASONE FUROATE 160,0 ug

150/50/160540876.87454/10.2.1/0876.874RegisteredNot 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: Indacaterol

    Consolidated Schedules 06 July 2026, line 6742

  • S4: Mometasone furoate

    • except when intended for inhalation or nasal administration.

    Consolidated Schedules 06 July 2026, line 7167

  • S3: Glycopyrronium

    Consolidated Schedules 06 July 2026, line 3691

  • S3: Indacaterol

    Consolidated Schedules 06 July 2026, line 3778

  • S3: Mometasone furoate

    • when intended for inhalation or nasal administration, except when intended for nasal administration as an aqueous spray, other than by pressurized aerosol, and indicated for the treatment of the symptoms of seasonal or perennial allergic rhinitis (hay fever) in adults and children between the age of 2 and 11 years of age, subject to
    • a maximum dose of 200 micrograms per nostril in adults and 50 micrograms per nostril in children; and
    • a maximum pack size of 200 doses. (S2, S4)

    Consolidated Schedules 06 July 2026, lines 3960 to 3965

  • S2: Mometasone furoate

    • when intended for nasal administration as an aqueous spray, other than by pressurized aerosol, and indicated for the treatment of the symptoms of seasonal or perennial allergic rhinitis (hay fever) in adults and children between the age of 2 and 11 years of age, subject to
    • a maximum dose of 200 micrograms per nostril in adults and 50 micrograms per nostril in children; and
    • a maximum pack size of 200 doses. (S3, S4)

    Consolidated Schedules 06 July 2026, lines 2284 to 2290

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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