Tobramycin inhalation solution gets tentative FDA approval

According to the FDA, the agency has issued a tentative approval of an application by PulmoFlow, Inc. to market tobramycin 300 mg/5 ml inhalation solution.

PulmoFlow, Inc. was established in Virginia in 2013. The company’s web site is a single page that says “PulmoFlow is a newly established company currently focused on solutions to improve the lives of patients with acute and chronic respiratory indications.” Also, according to the site, the company is “a dedicated licensing entity with a focus on pediatric, respiratory, and orphan indications” and is open to “possibilities of collaboration.”

A number of trademark applications for the name “PulmoFlow” have been submitted by PARI over the years, and PulmoFlow GmbH is listed at the same address as PARI GmbH.

Share

published on

May 10-May 14RDD 2026, Phoenix, AZ, USA

May 15-May 16: ATS Respiratory Innovation Summit 2026, Orlando, FL, USA

May 17-May 20: ATS International Conference 2026, Orlando, FL, USA

June 10SMI.London 2026, London, UK

July 13-July 162026 ISAM Congress, Taipei, Taiwan