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fluticasone propionate/formoterol fumarate dihydrate (Flutiform®)

 

Status: Medicine does not meet criteria for AWMSG assessment

Excluded from appraisal by AWMSG as meets exclusion criteria 5. See AWMSG criteria for appraising a medicine (PDF, 430Kb) for information.

Medicine details

Medicine name fluticasone propionate/formoterol fumarate dihydrate (Flutiform®)
Formulation 50 mcg/5 mcg, 125 mcg/5 mcg and 250 mcg/10 mcg metered dose inhaler
Reference number 2835
Indication

Regular treatment of asthma where the use of a combination product (an inhaled corticosteroid and a LABA) is appropriate for patients aged 5 years and above who are not adequately controlled with inhaled corticosteroids and 'as required' inhaled short-acting β2 agonist or for patients already adequately controlled on both an inhaled corticosteroid and a long-acting β2 agonist

Company Napp Pharmaceuticals Ltd
BNF chapter Respiratory system
Submission type N/A
Status Medicine does not meet criteria for AWMSG assessment
Date of issue 28/02/2018
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