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Warner Chilcott Announces FDA Approval of Next Generation Actonel
Date:10/11/2010

nopausal osteoporosis in the United States.  The product will be marketed as ATELVIA™ (risedronate sodium) delayed-release tablets.  

"The approval of ATELVIA represents an exciting addition to the ACTONEL franchise, as well as our women's healthcare product portfolio.  We believe the dosing convenience of ATELVIA sets it apart from other treatment options for osteoporosis patients and provides an opportunity to regain market share in the U.S. in this segment," said Roger Boissonneault, President and CEO of Warner Chilcott.

The Company anticipates the commercial launch of ATELVIA in early 2011.

About ATELVIAATELVIA is a bisphosphonate in a delayed-release formulation and is indicated for treatment of postmenopausal osteoporosis.  For information on dosage and administration, contraindications, warnings and precautions, adverse reactions, and other important safety and other prescribing information, please see http://www.wcrx.com/pdfs/pi/pi_atelvia.pdf.

About Warner Chilcott Warner Chilcott is a leading specialty pharmaceutical company currently focused on the gastroenterology, women's healthcare, dermatology and urology segments of the North American and Western European pharmaceuticals markets.  The Company is fully integrated with internal resources dedicated to the development, manufacturing and promotion of its products.  WCRX-G.

Forward Looking Statements This press release contains forward-looking statements concerning our operations, our anticipated financial performance and financial condition, and our business plans and growth strategy and product development efforts.  These statements constitute forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934.  The words "may," "might," "will," "should," "estimate," "proj
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SOURCE Warner Chilcott plc
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