Ikaria is committed to continually improving delivery systems for safe dosing and administration of INOMAX

INOMAX Delivery Systems
 

INOMAX® is a vasodilator, which, in conjunction with ventilatory support and other appropriate agents, is indicated for the treatment of term and near-term (>34 weeks gestation) neonates with hypoxic respiratory failure associated with clinical or echocardiographic evidence of pulmonary hypertension, where it improves oxygenation and reduces the need for extracorporeal membrane oxygenation.

INOMAX Important Safety Information (ISI)
INOMAX should not be used in the treatment of neonates known to be dependent on right-to-left shunting of blood

Read Full ISI
 

INOMAX Delivery Systems

The Food and Drug Administration (FDA) requires that INOMAX (nitric oxide) for inhalation be delivered through special drug delivery systems that meet specific criteria.

INOMAX delivery systems:

  • Allow for operator-determined concentrations of nitric oxide in the breathing circuit
  • Provide for a concentration that is constant throughout the respiratory cycle
  • Monitor for nitric oxide (NO), oxygen (O2), and nitrogen dioxide (NO2)
  • Prevent generation of excessive inhaled NO2
  • Meet all FDA-required specifications
INOmax DSIR INOmax DS INOvent
INOmax DSIR
offers functional enhancements
to INOmax DS.
INOmax DS
developed for bedside or transport situations.
INOvent
a bedside delivery system for INOMAX.

References

 

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Disclaimer

*Please note: When you access these resources, you are leaving the INOMAX website. Therefore, INOMAX and Ikaria Holdings Inc. do not endorse the accuracy of the information you may find. We encourage you to talk to your doctor about the accuracy of any information you discover through these Internet resources.

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