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Irish Medicines Database · HPRA register

Flutiform 50 microgram/5 microgram per metered dose pressurised inhalation, suspension

Authorisation PA1688/013/001 · Mundipharma Pharmaceuticals Limited

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Flutiform 50 microgram/5 microgram per metered dose pressurised inhalation, suspension
Licence PA1688/013/001 · Marketed
Licence holder
Mundipharma Pharmaceuticals Limited (all products →)
Active substances
Fluticasone propionate, Formoterol fumarate dihydrate
Dosage form
Pressurised inhalation, suspension
Route of administration
Inhalation use
ATC codes
R03AK, R03AK11
First authorised
19/10/2012
Prescription status
Product subject to prescription which may be renewed (B)
Supply
Supply through pharmacies only
Legal basis
Fixed combination application (Article 10b of Directive No 2001/83/EC)

Data: Health Products Regulatory Authority (HPRA) open dataset, licensed CC BY 4.0, published 04 Jul 2026. This listing is regulatory information, not medical advice — consult the package leaflet, SPC, or a healthcare professional. For the authoritative record see the HPRA register.