Regulatory PathRegulatory requirements compared

Active substances

Fluticasone + Formoterol

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
FLUTIFORM 125/5 mcg pressurised inhalation suspension0.125,0.005 mg,mgPressurised inhalation, suspension · Inhalation use1 InhalerSAR 130.00NCE · PrescriptionNapp pharmacuticals limited UKValid
FLUTIFORM 250/10 mcg pressurised inhalation suspension0.25,0.01 mg,mgPressurised inhalation, suspension · Inhalation use1 InhalerSAR 225.00NCE · PrescriptionNapp pharmacuticals limited UKValid
FLUTIFORM 50/5 mcg pressurised inhalation suspension0.05,0.005 mg,mgPressurised inhalation, suspension · Inhalation use1 InhalerSAR 105.00NCE · PrescriptionNapp pharmacuticals limited UKValid
Indications — CHI Daman Drug Formulary

ASTHMA

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
NHS Drug TariffFluticasone 125micrograms/dose / Formoterol 5micrograms/dose inhaler CFC free£28.00120 dose1 Oct 2026
NHS Drug TariffFluticasone 250micrograms/dose / Formoterol 10micrograms/dose inhaler CFC free£45.56120 dose1 Oct 2026
NHS Drug TariffFluticasone 50micrograms/dose / Formoterol 5micrograms/dose inhaler CFC free£14.40120 dose1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

WHO WHO Model List of Essential Medicines (2025)

  • 25.1. Antiasthmatic and medicines for chronic obstructive pulmonary disease · core
    Therapeutic equivalent to budesonide + formoterol for Asthma

Components

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.