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Perrigo Announces FDA Final Approval for Polyethylene Glycol 3350
Date:10/6/2009

ALLEGAN, Mich., Oct. 6 /PRNewswire-FirstCall/ -- Perrigo Company (Nasdaq: PRGO;TASE) today announced that it has received final approval from the U.S. Food and Drug Administration for its Abbreviated New Drug Application for over-the-counter (OTC) Polyethylene Glycol 3350, Powder for Solution. Perrigo is expecting to begin shipping immediately.

The product will be marketed under store brand labels and is comparable to Schering-Plough HealthCare Products' MiraLAX(®), indicated for the treatment of occasional constipation. Estimated brand sales for the product for the last 12 months ending August 28, 2009 were $200 million.

Perrigo's Chairman and CEO Joseph C. Papa stated, "This is another example of Perrigo's continuing commitment to innovation and bringing new products to market. It is investments like this that help save OTC healthcare consumers more than an estimated $1 billion annually when compared to the higher priced national brands."

Perrigo Company is a leading global healthcare supplier that develops, manufactures and distributes OTC and generic prescription pharmaceuticals, nutritional products, active pharmaceutical ingredients (API) and consumer products. The Company is the world's largest manufacturer of OTC pharmaceutical products for the store brand market. The Company's primary markets and locations of manufacturing and logistics operations are the United States, Israel, Mexico and the United Kingdom. Visit Perrigo on the Internet (http://www.perrigo.com).

Note: Certain statements in this press release are forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and are subject to the safe harbor created thereby. These statements relate to future events or the Company's future financial performance and involve known and unknown risks, uncertainties and other factors that may cause the
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