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December 17, 2012
08:04 EDTIRWD, FRXIronwood, Forest announce U.S. availability of LINZESS
Ironwood Pharmaceuticals (IRWD) and Forest Laboratories (FRX) announced today that LINZESS is now available in pharmacies throughout the United States. The U.S. Food and Drug Administration recently approved LINZESS as a once-daily oral capsule for adult men and women suffering from irritable bowel syndrome with constipation or chronic idiopathic constipation.
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April 17, 2014
16:08 EDTFRXActavis, Forest Labs receive second request under Hart-Scott-Rodino from FTC
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April 9, 2014
05:50 EDTFRXForest Labs reports FDA provided feedback on combination aclidinium, formoterol
Forest Laboratories announced that they have recently received feedback from the FDA regarding the fixed dose combination of aclidinium and formoterol. Although no new issues have arisen, further discussion is needed with the Agency in order to address questions related to CMC, or Chemistry, Manufacturing and Control, and a Type C meeting with the FDA is going to be requested, likely to be held during Q3 this year. Forest and Almirall believe that the fixed dose combination of aclidinium and formoterol can be an important therapy for U.S. COPD patients.

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