Regulatory

The FDA has approved Teva’s ProAir HFA albuterol metered dose inhaler with a dose counter for the treatment and prevention of bronchospasm in patients 4 years of age and older. According to the company, the… Read more . . .

The FDA has issued a warning letter to Breathable Foods, the manufacturer of AeroShot inhalable caffeine for “false or misleading statements in the labeling of their product.” The agency is also questioning the safety of… Read more . . .

The FDA has approved MedImmune’s FluMist Quadrivalent for the prevention of influenza, making the intranasal vaccine the first approved quadrivalent flu vaccine in the US. FluMist Quadrivalent contains two type A strains and type B… Read more . . .

Forest Laboratories has received EMA approval to market Colobreathe dry powder colistimethate sodium inhalation powder for the treatment of P. aeruginosa infections in cystic fibrosis patients aged 6 years and older, according to the company.… Read more . . .

The FDA’s Pulmonary-Allergy Drugs Advisory Committee (PADAC) has voted 12 to 2 in favor of approval for Forest Laboratories’ and Almirall’s NDA for a 400 μg twice daily dose aclidinium bromide inhalation powder to treat… Read more . . .

Among the warning letters posted to the FDA website on February 21, 2012 is a letter to FSC Laboratories dated June 9, 2011 detailing violations related to quality controls for the manufacture of the E-Z… Read more . . .

The FDA’s Pulmonary-Allergy Drugs Advisory Committee (PADAC) will meet on Thursday, February 23 to decide whether or not to approve Forest Labs’ aclidinium bromide inhalation powder for the treatment of COPD. Forest submitted an NDA… Read more . . .

According to the Associated Press, the FDA will investigate the safety of Aeroshot inhalable caffeine and whether the product can be considered a dietary supplement as the manufacturer claims or if it is subject to… Read more . . .

Alexza Pharmaceuticals says that the Day 80 Assessment Report it has received from the European Medicines Agency (EMA) regarding its Marketing Authorization Application (MAA) for Adasuve Staccato loxapine indicates that the report “outlines major objections… Read more . . .