ADASUVE

This brand name is authorized in Austria, Estonia, Spain, Hong Kong, Croatia, Ireland, Lithuania, Poland, Romania, Turkey, United Kingdom, United States

Active ingredients

The drug ADASUVE contains one active pharmaceutical ingredient (API):

1 Loxapine
UNII LER583670J - LOXAPINE

Loxapine binds with noradrenergic, histaminergic, and cholinergic receptors, and its interaction with these systems may influence the spectrum of its pharmacological effects. Loxapine is indicated for the rapid control of mild-to-moderate agitation in adult patients with schizophrenia or bipolar disorder.

Read about Loxapine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ADASUVE Inhalation powder European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
N05AH01 Loxapine N Nervous system → N05 Psycholeptics → N05A Antipsychotics → N05AH Diazepines, oxazepines and thiazepines
Discover more medicines within N05AH01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1608915, 1608926, 1650507, 1650518
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 113823002
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 326880
Country: HK Department of Health Drug Office Identifier(s): 67228
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1069358, 1069359, 1072654, 1072655
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100308516, 100308522
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W62549001, W62549002, W62550001, W62550002
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699587554079, 8699587554086
Country: US FDA, National Drug Code Identifier(s): 10885-003

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