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Ranbaxy Gets U.S. FDA Nod For Imitrex After Four Months Of Waiting

This article was originally published in PharmAsia News

Executive Summary

MUMBAI - Four months after the U.S. FDA imposed an import alert on 33 products manufactured by Ranbaxy, the company received a much needed shot in the arm after the drug regulator approved launch of its generic versions of GlaxoSmithKline's migraine drug Imitrex (sumatriptan) 100 mg, which has sales of over $1.1 billion in the U.S. alone

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