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Toggle Summary Taro Receives Approval for Terconazole Vaginal Cream, 0.4% ANDA; Generic Equivalent to Terazol-R- 7 Vaginal Cream
HAWTHORNE, N.Y.--(BUSINESS WIRE)--Jan. 20, 2005--Taro Pharmaceutical Industries Ltd. (Nasdaq: TARO) and its affiliates and subsidiaries ("Taro") reported today that it has received approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug Application ("ANDA") for
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Toggle Summary Taro Receives Approval for Hydrocortisone Butyrate Ointment, 0.1% ANDA: Generic Equivalent to Locoid(r) Ointment
HAWTHORNE, N.Y., Dec. 27, 2004 (PRIMEZONE) -- Taro Pharmaceutical Industries Ltd. (Nasdaq:TARO) reported today that it has received approval from the U.S. Food and Drug Administration for its Abbreviated New Drug Application ("ANDA") for Hydrocortisone Butyrate Ointment, 0.1%.
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Toggle Summary Taro to Supply Generic Elocon-R-to Clay Park in the U.S.
HAWTHORNE, N.Y.--(BUSINESS WIRE)--Dec. 23, 2004--Taro Pharmaceutical Industries Ltd. (Nasdaq: TARO) and its affiliates and subsidiaries ("Taro") announced today that it will supply Agis Industries (1983) Ltd. ("Agis") and its subsidiary, Clay Park Labs, Inc.
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Toggle Summary Taro USA Receives Approval for Halobetasol Propionate Ointment, 0.05% ANDA: Company Also Receives Tentative Approval for Gabapentin Oral Solution, 250 mg/5 mL ANDA
HAWTHORNE, N.Y., Dec. 16, 2004 (PRIMEZONE) -- Taro Pharmaceutical Industries Ltd. (Nasdaq:TARO) reported today that Taro Pharmaceuticals U.S.A., Inc. ("Taro USA"), its U.S. affiliate, has received approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug Application
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Toggle Summary Taro USA Receives Tentative Approval for Mometasone Furoate Topical Solution USP, 0.1% -Lotion- ANDA
HAWTHORNE, N.Y.--(BUSINESS WIRE)--Dec. 6, 2004--Taro Pharmaceutical Industries Ltd. (Nasdaq: TARO) reported today that Taro Pharmaceuticals U.S.A., Inc. ("Taro USA"), its U.S. affiliate, has received tentative approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug
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Toggle Summary Taro USA Receives Approval For Mometasone Furoate Ointment USP, 0.1% ANDA: Company Also Receives Tentative Approval for Mometasone Furoate Cream USP, 0.1% ANDA
HAWTHORNE, N.Y., Dec. 6, 2004 (PRIMEZONE) -- Taro Pharmaceutical Industries Ltd. (Nasdaq:TARO) reported today that Taro Pharmaceuticals U.S.A., Inc. ("Taro USA"), its U.S. affiliate, has received approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug Application
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Toggle Summary Taro Reports `A+' Bond Rating In Israel
HAWTHORNE, N.Y., Nov. 22, 2004 (PRIMEZONE) -- Taro Pharmaceutical Industries Ltd. ("Taro," "the Company," (Nasdaq:TARO)) today reported that it has received an "A+" rating from Maalot, the Israeli affiliate of Standard & Poor's, based on the rating standard employed in Israel, for the issuance of
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Toggle Summary Taro Reports Third Quarter and Nine Month 2004 Results; 3rd Quarter Results Reflect Return to Profitability and Improved Sales vs. 2nd Quarter 2004
HAWTHORNE, N.Y.--(BUSINESS WIRE)--Oct. 28, 2004--Taro Pharmaceutical Industries Ltd. ("Taro," the "Company," Nasdaq: TARO) today reported results for the Company's third quarter and the nine-month period ended September 30, 2004. Third Quarter 2004 Results Taro's third quarter sales were $73.3
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Toggle Summary Taro to Report 3rd Quarter 2004 Results and Conduct Conference Call on October 28, 2004
HAWTHORNE, N.Y.--(BUSINESS WIRE)--Oct. 26, 2004--Taro Pharmaceutical Industries Ltd. (Nasdaq:TARO) intends to report financial results for the third quarter of 2004 prior to the Nasdaq market opening on Thursday, October 28, 2004. The Company will conduct a conference call to discuss the results on
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Toggle Summary Taro Announces Approvals of ANDAs for Betamethasone Dipropionate Ointment (Augmented) and Ciprofloxacin Tablets
HAWTHORNE, N.Y., Oct. 13, 2004 (PRIMEZONE) -- Taro Pharmaceutical Industries Ltd. ("Taro") (Nasdaq:TARO) reported today that Taro Pharmaceuticals U.S.A., Inc. ("Taro USA"), its U.S. affiliate, has received approval from the U.S. Food and Drug Administration ("FDA") for its Abbreviated New Drug
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