INOMAX

This brand name is authorized in Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Poland, Romania, United States

Active ingredients

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

1 Nitric oxide (NO)
UNII 31C4KY9ESH - NITRIC OXIDE

Nitric oxide is a compound produced by many cells of the body. It relaxes vascular smooth muscle by binding to the haeme moiety of cytosolic guanylate cyclase. When inhaled, nitric oxide produces selective pulmonary vasodilation.

Read about Nitric oxide (NO)

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
INOMAX Inhalation gas 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
R07AX01 Nitric oxide R Respiratory system → R07 Other respiratory system products → R07A Other respiratory system products → R07AX Other respiratory system products
Discover more medicines within R07AX01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02270846
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 992-MEE-0515
Country: EE Ravimiamet Identifier(s): 1205301, 1205312, 1526509, 1526510
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 01194001, 01194002, 01194003, 01194004
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 142123, 450993
Country: FR Base de données publique des médicaments Identifier(s): 65795991, 68961183
Country: IT Agenzia del Farmaco Identifier(s): 035494018, 035494020, 035494032, 035494044
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1028424, 1028425, 1060179, 1060180
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100121143, 100310980
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W63527001, W63527002, W63767001
Country: US FDA, National Drug Code Identifier(s): 64693-002

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