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New Drug Applications, FDA Approvals, Approved Acquisitions, Divestitures and Licensing Agreements - Research Report on Merck, Allergan, Mylan, AstraZeneca, and GlaxoSmithKline
Date:9/16/2013

013-09-11/MRK">http://www.investorsreports.com/report/2013-09-11/MRK]

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Allergan Inc. Research Report

On September 11, 2013, Allergan Inc. (Allergan) announced that the US Food and drug Administration (FDA) has approved the marketing of its BOTOX Cosmetic (onabotulinumtoxinA), for an additional indication to temporarily treat moderate to severe lateral canthal lines, commonly known as "crow's feet" lines. Scott W. Whitcup M.D., Executive Vice President, Research and Development, Chief Scientific Officer at Allergan, said,  "We are pleased that the FDA has approved a new indication for BOTOX Cosmetic to temporarily improve the appearance of crow's feet lines. With this approval, BOTOX Cosmetic is now the only pharmaceutical approved to treat both crow's feet lines and frown lines between brows. This approval will enhance our ability to work with and train aesthetic physicians on the science of administering BOTOX Cosmetic to yield the best possible outcomes for patients." The Full Research Report on Allergan Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.investorsreports.com/report/2013-09-11/AGN]

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Mylan, Inc. Research Report

On September 3, 2013, Mylan Inc. (Mylan) announced that India's Foreign Investment Promotion Board (FIPB) and Cabinet Committee on Economic Affairs (CCEA) have approved its proposed acquisition of the Agila injectables businesses from Strides Arcolab Limited. Mylan's CEO, Heather Bresch commented, "We are very pleased to have received all outstanding Indian pre-merger regulatory approvals for the Agila transaction, especially considering the increased government regulation and oversight with respect to foreign investment in India. W
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