Jan 21 2010
Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) announced today that
the U.S. Food and Drug Administration (FDA) has granted tentative
approval for the Company's Abbreviated New Drug Application (ANDA) to
market its generic version of Novartis’ breast cancer treatment Femara®
(letrozole) Tablets, 2.5 mg. Final approval of Teva’s Letrozole Tablets
is expected upon expiry of patent protection for the brand product in
June 2011.
The brand product had annual sales of approximately $556 million in the
United States, based on IMS sales data.
Source:
Teva Pharmaceutical Industries Ltd.,