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Ranbaxy receives US FDA tentative approval for esomeprazole caps

Our Bureau, MumbaiThursday, February 7, 2008, 08:00 Hrs  [IST]

Ranbaxy Laboratories Limited (RLL) has received tentative approval from the US Food and Drug Administration for esomeprazole magnesium delayed-release capsules, 20 mg (base) and 40 mg (base). Astra Zeneca's Nexium (esomeprazole) is the second largest selling drug in USA with total annual market sales of $5.5 billion (IMS - MAT: December 2007). Esomeprazole is indicated for the short-term treatment (4 to 8 weeks) in the healing and symptomatic resolution of diagnostically confirmed erosive esophagitis, to maintain symptom resolution and healing of erosive esophagitis and for treatment of heartburn and other symptoms associated with Gastroesophageal Reflux Disease (GERD). Ranbaxy believes that it has a FTF (First to File) status on the drug, providing it with a potential 180 days marketing exclusivity, thereby offering a significant opportunity in the future. Ranbaxy Pharmaceuticals Inc. (RPI) based in Jacksonville, Florida, is a wholly owned subsidiary of Ranbaxy Laboratories Limited (RLL), India's largest pharmaceutical company. RPI is engaged in the sale and distribution of generic and branded prescription products in the US healthcare system.

 
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