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United States : LAUNCH of Donepezil Hydrochloride declared by Dr. Reddys.

After the approval by the United States Food & Drug Administration (USFDA) of Dr. Reddy's ANDA for Donepezil Hydrochloride Tablets, 23 mg, the Dr. Reddy's Laboratories (NYSE: RDY) has introduced Donepezil Hydrochloride Tablets, 23 mg, a therapeutic equivalent generic version of ARICEPTA, 23 mg in the US market on July 27, 2013.

As per the IMS Health the ARICEPTA, 23 mg brand had U.S. sales of about $92.6 Million MAT for the most latest twelve months ending in May 2013.

Dr. Reddy's Donepezil Hydrochloride Tablets, 23 mg is obtainable in bottle count sizes of 30 and 90.

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Publication:Mena Report
Date:Aug 19, 2013
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