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Shire Announces That The US Food And Drug Administration Has Responded To Its Citizen Petition For Adderall XR And Has Approved One Abbreviated New Drug Application For Generic Adderall XR

Statements included herein that are not historical facts are forward-looking statements. Such forward-looking statements involve a number of risks and uncertainties and are subject to change at any time. In the event such risks or uncertainties materialize, the Company's results could be materially adversely affected. The risks and uncertainties include, but are not limited to, risks associated with: the inherent uncertainty of research, development, approval, reimbursement, manufacturing and commercialization of the Company's Specialty Pharmaceuticals, Human Genetic Therapies and Regenerative Medicine products, as well as the ability to secure new products for commercialization and/or development; government regulation of the Company's products; the Company's ability to manufacture its products in sufficient quantities to meet demand; the impact of competitive therapies on the Company's products; the Company's ability to register, maintain and enforce patents and other intellectual property rights relating to its products; the Company's ability to obtain and maintain government and other third-party reimbursement for its products; and other risks and uncertainties detailed from time to time in the Company's filings with the Securities and Exchange Commission.

For further information please contact: Investor Relations:         Eric Rojas     erojas@shire.com +1-781-482-0999 Sarah Elton-Farr     seltonfarr@shire.com +44-1256-894157 Media:         Jessica Mann (Corporate)     jmann@shire.com +44-1256-894-280 Gwen Fisher (Specialty Pharma)     gfisher@shire.com +1-484-595-9836

SOURCE Shire plc

Copyright 2011 PR Newswire. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.
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