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Perrigo Company Announces FDA Approval for Ciclopirox Topical Solution
Date:9/19/2007

ALLEGAN, Mich., Sept. 19 /PRNewswire-FirstCall/ -- The Perrigo Company (Nasdaq: PRGO; TASE) today announced that it has received final approval from the U.S. Food and Drug Administration to manufacture and market Ciclopirox Topical Solution, 8% (Nail Lacquer). Shipments will begin immediately.

The product has been determined to be therapeutically equivalent (AT) to Sanofi Aventis US, LLC's Penlac(R) Nail Lacquer, indicated for the treatment of mild to moderate fungal infections of the fingernails and toenails. According to Wolters Kluwer data, brand sales for the last 12 months ending August, 2007 were $92 million.

Perrigo Company is a leading global healthcare supplier that develops, manufactures and distributes over-the-counter (OTC) and 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 facilities 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 actual results, levels of activity, performance or achievements of the Company or its industry to be materially different fro
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SOURCE Perrigo Company
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