AIRFLUSAL

This brand name is authorized in Albania, Austria, Germany, Estonia, Spain, Hong Kong, Croatia, Ireland, Italy, Lithuania, Malta, Netherlands, Poland, Romania, Singapore, United Kingdom, South Africa

Active ingredients

The drug AIRFLUSAL contains a combination of these active pharmaceutical ingredients (APIs):

1 Salmeterol
UNII 6EW8Q962A5 - SALMETEROL XINAFOATE

Salmeterol is a selective long-acting (12 hour) β2 adrenoceptor agonist. These pharmacological properties of salmeterol offer more effective protection against histamine-induced bronchoconstriction and produce a longer duration of bronchodilation, lasting for at least 12 hours, than recommended doses of conventional short-acting β2 agonists.

Read about Salmeterol
2 Fluticasone
UNII O2GMZ0LF5W - FLUTICASONE PROPIONATE

Fluticasone has anti-inflammatory and vasoconstrictive features. Fluticasone given by inhalation at recommended doses has a potent glucocorticoid anti-inflammatory action within the lungs, resulting in a reduction of both symptoms and exacerbations of asthma, with a lower incidence and severity of adverse effects than those observed when corticosteroids are administered systemically.

Read about Fluticasone

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
R03AK06 Salmeterol and fluticasone R Respiratory system → R03 Drugs for obstructive airway diseases → R03A Adrenergics, inhalants → R03AK Adrenergics and other drugs for obstructive airway diseases
Discover more medicines within R03AK06

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: AL Fondi i Sigurimit të Detyrueshëm të Kujdesit Shëndetësor Identifier(s): 515/237, 516/237
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 09121840, 09121857, 09121863, 11889956, 11889962, 11889979, 11889985, 13896972, 13896989, 14238774, 16395302, 16582062, 16803623, 16803646, 16803652, 16884254
Country: EE Ravimiamet Identifier(s): 1636466, 1636477, 1636488, 1636499, 1636501, 1636512, 1636523, 1636534, 1636545, 1636556
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 80248, 80249
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 309504, 342154, 342156, 377145, 377147, 377149
Country: HK Department of Health Drug Office Identifier(s): 63960, 63961, 63964
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-007513419, HR-H-597688265
Country: IE Health Products Regulatory Authority Identifier(s): 16005, 16011, 53487, 53488
Country: IT Agenzia del Farmaco Identifier(s): 043262029, 045152016, 045152081
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1072343, 1072344, 1074618, 1074619, 1074620, 1074621, 1074973, 1074974, 1074975, 1074976, 1079504, 1079505, 1082679, 1082680, 1082681, 1082682, 1082683, 1082684, 1082685, 1082686, 1082687, 1082688, 1082689, 1082690, 1082691, 1082692, 1082693, 1082694, 1082695, 1082696
Country: MT Medicines Authority Identifier(s): AA1122/02401, AA1122/02402
Country: NL Z-Index G-Standaard, PRK Identifier(s): 127663, 62529, 62537
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100356030, 100356053, 100365224, 100365230, 100443473, 100447270
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W60522001, W60522002, W60522003, W60522004, W60522005, W60522006, W60522007, W61757001, W61757002, W61757003, W61757004, W61757005, W61757006, W61757007
Country: SG Health Sciences Authority Identifier(s): 15523P
Country: ZA Health Products Regulatory Authority Identifier(s): 47/21.5.4/1320, 47/21.5.4/1321

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