AIRBUFO

This brand name is authorized in Austria, Croatia, Estonia, Germany, Ireland, Lithuania, Malta, Poland, Romania.

Active ingredients

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

1	Budesonide UNII Q3OKS62Q6X - BUDESONIDE
	Budesonide is a glucocorticosteroid with a high local anti-inflammatory effect. At doses clinically equivalent to systemically acting glucocorticosteroids, budesonide gives significantly less HPA axis suppression and has a lower impact on inflammatory markers.
	Read more about Budesonide
2	Formoterol fumarate dihydrate UNII W34SHF8J2K - FORMOTEROL FUMARATE
	Formoterol is a predominantly selective β2-stimulator. Formoterol has bronchodilator activity in patients with reversible obstructive airway diseases. In humans formoterol is effective in the prophylaxis of bronchospasm induced by methacholine challenge.
	Read more about Eformoterol

Medicine classification

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

ATC Group		Classification
R03AK07	Formoterol and budesonide	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 R03AK07

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	13584675, 13584681, 13584698, 13584706, 16756094, 16756102
EE	Ravimiamet	1742778, 1742789, 1742790, 1742802, 1742813, 1808603, 1808614, 1808625, 1808647
HR	Agencija za lijekove i medicinske proizvode	HR-H-623053682, HR-H-824195818
IE	Health Products Regulatory Authority	29234, 69933
LT	Valstybinė vaistų kontrolės tarnyba	1085616, 1085617, 1085618, 1085619, 1085620, 1092465, 1092466, 1092467, 1092468
MT	Medicines Authority	MA1122/02101, PI908/24501A
PL	Rejestru Produktów Leczniczych	100389561, 100431270
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W65024001, W65024002, W65024003, W65024004, W65024005, W67568001, W67568002, W67568003, W67568004