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Oct27
New Nexium® Formulation: NEXIUM® For Delayed-Release Oral Suspension, Approved by the USFDA

A new formulation of AstraZeneca (NYSE: AZN)’s prescription proton pump inhibitor -NEXIUM® (esomeprazole magnesium) - has recently been approved by the USFDA.

The new NEXIUM® For Delayed-Release Oral Suspension is now approved for the treatment of GERD, including symptomatic gastroesophageal reflux disease (GERD), healing and maintenance of healing of erosive esophagitis (EE), and risk reduction of NSAID-associated gastric (stomach) ulcers.

NEXIUM.jpgThe same active ingredient used in NEXIUM® Delayed-Release Capsules, esomeprazole, is contained in either 20 mg or 40 mg dosage in every packet of NEXIUM® For Delayed-Release Oral Suspension.

The only difference is that, in this new formulation, the esomeprazole granules and inactive granules are mixed with water to form a suspension and are given by oral, nasogastric or gastric administration.

The new formulation: NEXIUM® For Delayed-Release Oral Suspension will be available in the first quarter of 2007.

 

 

 

 

 

 

Find more details from the press release.

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« Clinical Data Demonstrating Additive Anti-Fibrotic Combination Effects of Actimmune® and Pirfenidone, Presented by InterMune, Inc. at CHEST 2006 | Main | Treatment Response to Mesalamine = Rapid Mucosal Healing in Moderately Active Ulcerative Colitis (UC) Patients, According to Combined Data Analysis »

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