News Release
                    
                U.S. Food and Drug Administration (FDA) Extends Review of Mallinckrodt’s New Drug Application for XARTEMIS™ XR (oxycodone hydrochloride and acetaminophen) Extended-Release Tablets (CII)
                    ST. LOUIS--(BUSINESS WIRE)--Nov. 25, 2013--
      Mallinckrodt
      (NYSE: MNK) today announced that the U.S. Food and Drug Administration
      (FDA) extended the review of the New Drug Application (NDA) for
      investigational compound XARTEMIS™ XR (oxycodone
      hydrochloride and acetaminophen) Extended-Release Tablets (CII).
      XARTEMIS XR, previously known as MNK-795, was studied for the management
      of moderate to severe acute pain where the use of an opioid analgesic is
      appropriate.
    
      The three-month extension from the FDA is in response to additional data
      submitted by Mallinckrodt. Mallinckrodt and the FDA have begun and will
      continue discussions regarding labeling as part of the application
      review throughout this period.
    
      “If approved, we believe that XARTEMIS XR could provide an important new
      option as an extended-release treatment for patients with acute pain,”
      said Mark Trudeau, President and Chief Executive Officer, Mallinckrodt.
      “As a leader in pain management, Mallinckrodt remains committed to
      developing medications that address the needs of patients, and will work
      with the FDA throughout the review of the XARTEMIS XR application.”
    
      XARTEMIS XR, an investigational, extended-release oral formulation of
      oxycodone and acetaminophen uses a dual layer delivery mechanism with
      both immediate- and extended-release components. In July, the FDA
      accepted for filing the NDA for XARTEMIS XR and granted priority review.
      There are currently no extended-release oxycodone/acetaminophen
      combinations on the market for the management of acute pain.
    
      ABOUT MALLINCKRODT:
    
      Mallinckrodt is a global specialty pharmaceutical business that
      develops, manufactures, markets and distributes specialty pharmaceutical
      products and medical imaging agents. The company’s Specialty
      Pharmaceuticals segment includes branded and generic drugs and active
      pharmaceutical ingredients, and the Global Medical Imaging segment
      includes contrast media and nuclear imaging agents. Mallinckrodt has
      approximately 5,500 employees worldwide and a commercial presence in
      roughly 70 countries. The company’s 2013 revenue totaled $2.2 billion.
      To learn more about Mallinckrodt, visit www.mallinckrodt.com.
    
      FORWARD-LOOKING STATEMENTS
    
      Any statements contained in this communication that do not describe
      historical facts may constitute forward-looking statements as that term
      is defined in the Private Securities Litigation Reform Act of 1995. Such
      forward-looking statements include, but are not limited to, statements
      about future financial condition and operating results, economic,
      business, competitive and/or regulatory factors affecting our business.
      Any forward-looking statements contained herein are based on our
      management's current beliefs and expectations, but are subject to a
      number of risks, uncertainties and changes in circumstances, which may
      cause actual results or Company actions to differ materially from what
      is expressed or implied by these statements. The factors that could
      cause actual future results to differ materially from current
      expectations include, but are not limited to, our ability to receive
      procurement and production quotas granted by the U.S. Drug Enforcement
      Administration, our ability to obtain and/or timely transport
      molybdenum-99 to our technetium-99m generator production facilities,
      customer concentration, cost-containment efforts of customers,
      purchasing groups, third-party payors and governmental organizations,
      our ability to successfully develop or commercialize new products, our
      ability to protect intellectual property rights, competition, our
      ability to integrate acquisitions of technology, products and
      businesses, product liability losses and other litigation liability, the
      reimbursement practices of a small number of large public or private
      issuers, complex reporting and payment obligation under healthcare
      rebate programs, changes in laws and regulations, conducting business
      internationally, foreign exchange rates, material health, safety and
      environmental liabilities, litigation and violations and information
      technology infrastructure. These and other factors are identified and
      described in more detail in the “Risk Factors” section of the Form 10
      Registration Statement, as amended. We disclaim any obligation to update
      these forward-looking statements other than as required by law.
    

Source: Mallinckrodt
      Mallinckrodt
Lynn Phillips, 314-654-3263
Manager, Media
      Relations
lynn.phillips@mallinckrodt.com
or
Meredith
      Fischer, 314-654-3318
Senior Vice President, Communications
meredith.fischer@mallinckrodt.com
or
John
      Moten, 314-654-6650
Vice President, Investor Relations
john.moten@mallinckrodt.com