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2013 | 2012 | 2011 | 2010 | 2009 | 2008
DateTitle 
12/31/09Taro Reports Voting Results from Its Annual General MeetingPrinter Friendly Version
12/18/09Taro Announces Clinical Trials with T2007, Its Second Proprietary Non-Sedating Barbiturate DrugPrinter Friendly Version
12/10/09Taro Sends Important Update to ShareholdersPrinter Friendly Version
12/08/09Taro Sends Letter to Update ShareholdersPrinter Friendly Version
12/04/09FDA Approves Initiation of Clinical Studies in the U.S. for T2000, Taro's Proprietary Non-Sedating Barbiturate CompoundPrinter Friendly Version
12/02/09Taro Provides Preliminary Third Quarter and Year-to-Date 2009 Financial ResultsPrinter Friendly Version
09/29/09Taro Files Lawsuit Against Sun in U.S. Federal CourtPrinter Friendly Version
09/11/09Taro Announces Postponement of September 13, 2009 Shareholders MeetingPrinter Friendly Version
08/10/09Taro Provides Preliminary First Half 2009 Financial ResultsPrinter Friendly Version
07/27/09Taro Sues Synerx Pharma, Karalex Pharma and DPT Laboratories for Patent InfringementPrinter Friendly Version
07/27/09Taro Receives FDA Approval for Cetirizine Hydrochloride Tablets (OTC) ANDAPrinter Friendly Version
07/15/09Taro Receives Patent for Ovide(R)Printer Friendly Version
06/11/09Taro Announces Preliminary Court Approval of Settlement in Securities LawsuitPrinter Friendly Version
06/10/09Taro and Quinnova Announce Agreement to Co-Promote "Neosalus" and "Cleanse & Treat" in the United StatesPrinter Friendly Version
05/22/09Taro Provides Preliminary First Quarter 2009 Financial ResultsPrinter Friendly Version
05/22/09Taro to Restate Financial Results for 2004 and 2005; Revises 2006, 2007 and 2008 Estimated Financial ResultsPrinter Friendly Version
05/21/09Taro Receives FDA Approval for Sulfacetamide Sodium Topical Suspension ANDAPrinter Friendly Version
04/03/09Taro Receives Final FDA Approval for Carbamazepine Extended-Release TabletsPrinter Friendly Version
02/11/09Taro Receives FDA Approval for Levetiracetam Oral SolutionPrinter Friendly Version
02/06/09Taro Receives FDA Warning Letter Following Inspection of Its Canadian Manufacturing FacilityPrinter Friendly Version
02/05/09Taro Receives Final FDA Approval for Lamotrigine Chewable Tablets ANDAPrinter Friendly Version
02/02/09Taro Provides Preliminary 2008 Full Year ResultsPrinter Friendly Version
01/28/09Taro Receives Final FDA Approval for Lamotrigine Tablets ANDAPrinter Friendly Version
01/06/09Sun Refuses to Accept Taro's Offer to MediatePrinter Friendly Version
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