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Fluticasone propionate 50 micrograms/actuation, nasal spray, suspension

Haleon Ireland LimitedPA0678/118/001

Main Information

Trade NameFluticasone propionate 50 micrograms/actuation, nasal spray, suspension
Active SubstancesFluticasone propionate (micronised)
Dosage FormNasal spray, suspension
Licence HolderHaleon Ireland Limited
Licence NumberPA0678/118/001

Group Information

ATC CodeR01AD Corticosteroids
R01AD08 fluticasone


License statusAuthorised
Licence Issued12/06/2015
Legal statusProduct not subject to medical prescription
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to the general public
Conditions of LicenceRetail through pharmacies and promotion to the public if compliant with the following restrictions: pack containing not more than 3,000 mcg fluticasone proprionate, maximum period of treatment: 6 months, maxiumum dose: 100 mcg per nostril, maximum daily dose: 200 mcg per nostril, limited indications, pharmaceutical form: non-pressurised nasal spray, for use in adults only.
Marketing StatusNot marketed


Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available
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