Welcome to Taro Ireland

Taro Pharmaceuticals Ireland Ltd. is in the process of establishing operations in Pharmaceutical Research & Manufacturing at its new location in Roscrea, Co.Tipperary, Ireland.

Taro Pharmaceuticals Industries Ltd. looks forward to diversifying its presence in global markets with the added capabilities and technology at the Roscrea facility.

For employment opportunities, click here.



Press Releases

June 11, 2009
Taro Announces Preliminary Court Approval of Settlement in Securities Lawsuit
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June 10, 2009
Taro and Quinnova Announce Agreement to Co-Promote "Neosalus" and "Cleanse & Treat" in the United States
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May 22, 2009
Taro to Restate Financial Results for 2004 and 2005; Revises 2006, 2007 and 2008 Estimated Financial Results
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May 22, 2009
Taro Provides Preliminary First Quarter 2009 Financial Results
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April 03, 2009
Taro Receives Final FDA Approval for Carbamazepine Extended-Release Tablets
  Generic Equivalent to Novartis' Tegretol(r)-XR Tablets USP, 100 mg, 200 mg and 400 mg
HAWTHORNE, N.Y., Apr 3, 2009 (GlobeNewswire via COMTEX) -- Taro Pharmaceutical Industries Ltd. ("Taro" or the "Company") (Pink Sheets:TAROF) today reported that it received final approval from the U.S. Food and Drug Administration for its Abbreviated New Drug Application ("ANDA") for Carbamazepine Extended-Release Tablets USP, 100 mg, 200 mg and 400 mg ("carbamazepine extended-release tablets").

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February 11, 2009
Taro Receives FDA Approval for Levetiracetam Oral Solution

Generic Equivalent to UCB's Keppra(r) Oral Solution, 100 mg/mL

HAWTHORNE, N.Y., Feb. 11, 2009 (GlobeNewswire via COMTEX) -- Taro Pharmaceutical Industries Ltd. ("Taro," the "Company") (Pink Sheets:TAROF) reported today that it has received approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug Application ("ANDA") for Levetiracetam Oral Solution, 100 mg/mL ("levetiracetam oral solution").

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February 06, 2009
TARO RECEIVES FDA WARNING LETTER FOLLOWING INSPECTION OF ITS CANADIAN MANUFACTURING FACILITY

The Company has Already Taken Corrective Action Regarding Many of the Comments Contained in the Letter

HAWTHORNE, N.Y., Feb. 6, 2009 - Taro Pharmaceutical Industries Ltd. (“Taro,” the “Company,” Pink Sheets: TAROF) announced that yesterday, February 5, 2009, it received a warning letter from the U.S. Food and Drug Administration (“FDA”) regarding the inspection of the Company’s Canadian manufacturing facility in July 2008. This is the first such letter that the Company or any of its affiliates has ever received.

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February 05, 2009
Taro Receives Final FDA Approval for Lamotrigine Chewable Tablets ANDA
Generic Equivalent to GlaxoSmithKline's Lamictal(r) CD Tablets, 5 mg and 25 mg

HAWTHORNE, N.Y., Feb. 5, 2009 (GLOBE NEWSWIRE) -- Taro Pharmaceutical Industries Ltd. ("Taro," the "Company,") (Pink Sheets:TAROF) reported today that it has received final approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug Application ("ANDA") for Lamotrigine Tablets (Chewable Dispersible), 5 mg and 25 mg ("lamotrigine chewable tablets").

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February 02, 2009
Taro Provides Preliminary 2008 Full Year Results
Net Income in 2008 Increases 143% to $51 Million From $21 Million in 2007 $74 Million Net Cash Generated From Operations in 2008

HAWTHORNE, N.Y., Feb. 2, 2009 (GLOBE NEWSWIRE) -- Taro Pharmaceutical Industries Ltd. ("Taro," the "Company,") (Pink Sheets:TAROF) today provided preliminary, unaudited and unreviewed information on its financial performance for the year ended December 31, 2008.

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January 28, 2009
Taro Receives Final FDA Approval for Lamotrigine Tablets ANDA

Generic Equivalent to GlaxoSmithKline's Lamictal(r) Tablets, 25 mg, 100 mg, 150 mg and 200 mg

HAWTHORNE, N.Y., Jan. 28, 2009 (GLOBE NEWSWIRE) -- Taro Pharmaceutical Industries Ltd. ("Taro," the "Company,") (Pink Sheets:TAROF) reported today that it has received final approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug Application ("ANDA") for Lamotrigine Tablets 25 mg, 100 mg, 150 mg, and 200 mg ("Lamotrigine Tablets"). Taro had received tentative approval for this ANDA in March 2008.

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January 06, 2009
Sun Refuses to Accept Taro's Offer to Mediate
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