Taro Receives FDA Approval for Levetiracetam Tablets

-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 Tablets, 250 mg, 500 mg, 750 mg and 1000 mg (“levetiracetam tablets”).

Taro’s levetiracetam tablets is a prescription product used in the treatment of epilepsy, and is bioequivalent to UCB’s Keppra® Tablets. According to industry sources, levetiracetam tablets had U.S. sales of over $700 million in 2009.

Taro Pharmaceutical Industries Ltd. is a multinational, science-based pharmaceutical company, dedicated to meeting the needs of its customers through the discovery, development, manufacturing and marketing of the highest quality healthcare products.

For further information on Taro Pharmaceutical Industries Ltd., please visit the Company’s website at http://www.taro.com.

Press Release Source: Taro Pharmaceutical Industries Ltd. On Tuesday