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Budesonide, formoterol (Symbicord Turbuhaler 80: /Dose, Symbicord Turbuhaler 160: /Dose, Symbicord Turbuhaler 320: /Dose, Facet Turbuhaler 80: Dose, Facet Turbuhaler 160: Dose, Fcet Turbuhaler 320:, Vannair 80:4,5, Vannair 160:4,5)

Budesonide, formoterol

Astrazeneca Pharmaceuticals (Pty) Ltd

S4Read from the PI-PIL document and verified

Registration

Applicant
Astrazeneca Pharmaceuticals (Pty) Ltd
Registrations
8
Schedule source
SAHPRA documentation

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Symbicord turbuhaler 80:4,5 ug/dose

EACH DELIVERED DOSE CONTAINS BUDESONIDE 80,0 µg FORMOTEROL FUMARATE DIHYDRATE 4,5 µg

4,5 ug35040435/21.5.1/0404RegisteredNot determinedNone
Symbicord turbuhaler 160:4,5 ug/dose

EACH DELIVERED DOSE CONTAINS BUDESONIDE 160,0 ug FORMOTEROL FUMARATE DIHYDRATE 4,5 ug

4,5 ug35040535/21.5.1/405RegisteredNot determinedNone
Symbicord turbuhaler 320:9 ug/dose

EACH DELIVERED DOSE CONTAINS BUDESONIDE 320,0 ug FORMOTEROL FUMARATE 9,0 ug

9 ug38018738/21.5.1/0187RegisteredNot determinedNone
Facet turbuhaler 80:4,5 ug dose

EACH DELIVERED DOSE CONTAINS: BUDESONIDE 80,0 μg FORMOTEROL FUMARATE DIHYDRATE 4,5 μgNone

4,5 ug45025745/2.1/0257RegisteredNot determinedNone
Facet turbuhaler 160:4,5 ug dose

EACH DELIVERED DOSE CONTAINS: BUDESONIDE 160,0 μg FORMOTEROL FUMARATE DIHYDRATE 4,5 μg

4,5 ug45025845/21.5.1/0258RegisteredNot determinedNone
Fcet turbuhaler 320:9 ug

EACH DELIVERED DOSE CONTAINS: BUDESONIDE 320,0 μg FORMOTEROL FUMARATE DIHYDRATE 9,0 μg

9 ug45025945/21.5.1/0259RegisteredNot determinedNone
Vannair 80:4,5

EACH ACTUATION CONTAINS BUDESONIDE 80,0 ug FORMOTEROL FUMARATE 4,5 ug

80 μg, 160 μgInhalerA390506A39/21.5.1/0506Approved 16 October 2020RegisteredS4PI
Vannair 160:4,5

EACH ACTUATION CONTAINS BUDESONIDE 160,0 ug FORMOTEROL FUMARATE 4,5 ug

Not listedA390507A39/21.5.1/0507RegisteredNot determinedNone

Regulatory status

Where S4 sits on the scale

Prescription-only medicine.

Schedule 4 covers most ordinary prescription medicines. You need a prescription from an authorised prescriber, such as a doctor or dentist, and a pharmacist dispenses it. Its price, name, pack size and strength can still be told to the public, as long as nothing links it to what it treats.

Schedule S4, read from the product's PI-PIL leaflet.

Who may supply: A pharmacist dispensing against a written or verbal prescription from an authorised prescriber; a veterinarian, who may also prescribe, compound or dispense it directly; a medical practitioner or dentist, who may prescribe it and may compound or dispense it directly only if licensed under section 22C(1)(a); manufacturers and wholesalers may supply people who may lawfully possess it; and, for animal treatment, a person practising a para-veterinary profession, on a veterinarian's written or verbal instruction.

Consolidated Schedules listings for Budesonide, formoterol fumarate

  • S4: Budesonide

    • except when intended for the prophylaxis and treatment of seasonal and perennial allergic rhinitis in adults and children aged 12 years and older; (S2)
    • except when intended for inhalation or nasal administration, unless listed in another Schedule. (S3)

    Consolidated Schedules 06 July 2026, lines 5577 to 5582

  • S4: Formoterol

    Consolidated Schedules 06 July 2026, line 6443

  • S3: Budesonide

    • when intended inhalation or nasal administration, unless listed in another Schedule. (S4)
    • except when intended for the prophylaxis and treatment of seasonal and perennial allergic rhinitis in adults and children aged 12 years and older. (S2)

    Consolidated Schedules 06 July 2026, lines 3237 to 3242

  • S2: Budesonide

    • when intended for the prophylaxis and treatment of seasonal and perennial allergic rhinitis in adults and children aged 12 years and older; (S3)
    • except when intended for inhalation and nasal administration, unless listed in another Schedule. (S4)

    Consolidated Schedules 06 July 2026, lines 1696 to 1701

Pharmacological class: Corticosteroids and analogues. (class 21.5.1)

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.

Combination product

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

SAHPRA documents

Schedule verified from official documents

Schedule Verification

This medication's schedule (S4) has been verified from official SAHPRA documents with 90% confidence.

These documents are provided by SAHPRA for informational purposes. Always consult with a healthcare professional for medical advice.

Background

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Research articles

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