Dr.
Reddy’s Announces the Launch of Fenofibrate Capsules, USP 43 mg and 130 mg
Dr. Reddy’s Laboratories announced
today that it has launched Fenofibrate Capsules, USP 43 mg and 130 mg a
therapeutic equivalent generic version of ANTARA® (fenofibrate) capsules, in
the US market on April 22, 2014, approved by the United States Food & Drug
Administration (USFDA).
The ANTARA® (fenofibrate)
capsules brand and generic had U.S. sales of approximately $74 Million MAT for
the most recent twelve months ending in February 2014 according to IMS Health*.
Dr. Reddy’s Fenofibrate
capsules, USP 43 mg is available in bottle counts of 30 and 130 mg are
available in bottle counts of 30 and 90.
Disclaimer
This press release
includes forward-looking statements, as defined in the U.S. Private Securities
Litigation Reform Act of 1995. We have based these forward-looking statements
on our current expectations and projections about future events. Such
statements involve known and unknown risks, uncertainties and other factors
that may cause actual results to differ materially. Such factors include, but
are not limited to, changes in local and global economic conditions, our
ability to successfully implement our strategy, the market acceptance of and
demand for our products, our growth and expansion, technological change and our
exposure to market risks. By their nature, these expectations and projections
are only estimates and could be materially different from actual results in the
future.
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