Sandoz Canada has expanded its product range with the introduction of a new respiratory antibiotic, Tobramycin inhalation solution.

The medicine is an authorised generic version of Tobi that is currently marketed by Novartis Pharmaceuticals Canada.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

It is suggested for the management of cystic fibrosis patients with chronic pulmonary Pseudomonas aeruginosa (P aeruginosa) infections.

Cystic fibrosis is a life-threatening genetic disease that primarily affects the lungs and digestive system.

Sandoz Canada president Michel Robidoux said: "We are proud to bring an authorised generic version of Tobi to Canadian patients with cystic fibrosis and suffering from chronic pulmonary infections.

"This launch is in line with our commitment to offer high-quality, affordable medicines in order to facilitate patient access to healthcare."

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData
"We are proud to bring an authorised generic version of Tobi to Canadian patients with cystic fibrosis and suffering from chronic pulmonary infections."

Sandoz’s Tobramycin inhalation solution is a formulation of Tobramycin that is designed specifically for administration by inhalation.

Tobramycin is an aminoglycoside antibiotic derived from Streptomyces tenebrarius and is used to treat various types of bacterial infections.

When the medicine is inhaled, tobramycin can be detected at high concentrations in the sputum of cystic fibrosis patients. It is a cationic polar molecule that does not readily cross epithelial membranes and is chemically and pharmacologically related to the aminoglycoside class of antibiotics.

According to the company, the respiratory antibiotic’s primary mode of action is bactericidal resulting from disruption of protein synthesis in susceptible bacteria.

The safety and efficacy of the medicine was evaluated in two identically designed, double-blind, randomised, placebo-controlled 24-week clinical studies at 69 cystic fibrosis centres in the US.

Figures released by Cystic Fibrosis Canada show that more than 4,000 Canadian adults and children have the disease.

Pharmaceutical Technology Excellence Awards - The Benefits of Entering

Gain the recognition you deserve! The Pharmaceutical Technology Excellence Awards celebrate innovation, leadership, and impact. By entering, you showcase your achievements, elevate your industry profile, and position yourself among top leaders driving pharmaceutical advancements. Don’t miss your chance to stand out—submit your entry today!

Nominate Now