— If 510(k) cleared, this next-generation investigational inhaled nitric oxide delivery system would be the latest in a long line of dual channel delivery systems building on Company's dedication to meeting clinicians' evolving needs —
The safety and efficacy of the investigational inhaled nitric oxide delivery system has not been evaluated by the FDA.
INOmax® (nitric oxide) gas, for inhalation, is an FDA-approved treatment that is indicated to improve oxygenation and reduce the need for extracorporeal membrane oxygenation in term and near-term (>34 weeks gestation) neonates with hypoxic respiratory failure associated with clinical or echocardiographic evidence of pulmonary hypertension in conjunction with ventilatory support and other appropriate agents.1 Please see Important Safety Information for INOmax below.
"This FDA submission marks an important milestone in our commitment to providing advancements in the delivery of our products to help improve clinician experiences," said
If 510(k) cleared, the next-generation inhaled nitric oxide delivery system would be the latest in a long line of dual channel delivery systems; would combine automation, integration and interaction in one device; and build on Mallinckrodt's dedication to meeting clinicians' evolving needs.2
INOmax has a well-established efficacy and safety profile with more than 20 years on the market and over 875,000 patients treated globally.1,3
Mallinckrodt is committed to providing support to healthcare professionals utilizing the INOmax delivery systems. Mallinckrodt provides access to INOmax Total Care® offerings whose goal is to help critical care clinicians face unexpected challenges in the NICU by providing comprehensive, 24/7/365 service, device training, and INO delivery support when and where they need it. For more information about INOmax, please visit INOmax.com.
The investigational inhaled nitric oxide delivery system is not available for sale, distribution or use.
INOmax® (nitric oxide) gas, for inhalation, is indicated to improve oxygenation and reduce the need for extracorporeal membrane oxygenation in term and near-term (>34 weeks gestation) neonates with hypoxic respiratory failure associated with clinical or echocardiographic evidence of pulmonary hypertension in conjunction with ventilatory support and other appropriate agents.
IMPORTANT SAFETY INFORMATION
Please see Full Prescribing Information.
Globally, prescribing information varies; refer to the individual country product label for complete information.
Mallinckrodt is a global business consisting of multiple wholly owned subsidiaries that develop, manufacture, market and distribute specialty pharmaceutical products and therapies. The company's Specialty Brands reportable segment's areas of focus include autoimmune and rare diseases in specialty areas like neurology, rheumatology, hepatology, nephrology, pulmonology, ophthalmology, and oncology; immunotherapy and neonatal respiratory critical care therapies; analgesics; cultured skin substitutes and gastrointestinal products. Its Specialty Generics reportable segment includes specialty generic drugs and active pharmaceutical ingredients. To learn more about Mallinckrodt, visit www.mallinckrodt.com.
Mallinckrodt uses its website as a channel of distribution of important company information, such as press releases, investor presentations and other financial information. It also uses its website to expedite public access to time-critical information regarding the company in advance of or in lieu of distributing a press release or a filing with the U.S. Securities and Exchange Commission (SEC) disclosing the same information. Therefore, investors should look to the Investor Relations page of the website for important and time-critical information. Visitors to the website can also register to receive automatic e-mail and other notifications alerting them when new information is made available on the Investor Relations page of the website.
This release includes forward-looking statements concerning Mallinckrodt's s 510(k) premarket notification application and the Company's inhaled nitric oxide delivery system. The statements are based on assumptions about many important factors, including the following, which could cause actual results to differ materially from those in the forward-looking statements: satisfaction of regulatory and other requirements; actions of regulatory bodies and other governmental authorities; changes in laws and regulations; issues with product quality, manufacturing or supply, or patient safety issues; and other risks identified and described in more detail in the "Risk Factors" section of Mallinckrodt's most recent Annual Report on Form 10-K, Mallinckrodt's Quarterly Report on Form 10-Q for the quarterly period ended
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Mallinckrodt, the "M" brand mark and the Mallinckrodt Pharmaceuticals logo are trademarks of a Mallinckrodt company. Other brands are trademarks of a Mallinckrodt company or their respective owners. ©2022 Mallinckrodt. US-2200202 09/22
1 INOmax. Package Insert.
2 Data on File - Ref-05943. Mallinckrodt Pharmaceuticals.
3 Data on File - Ref-01753. Mallinckrodt Pharmaceuticals.
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