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Fort Dodge Animal Health Announces Reintroduction of ProHeart 6 to the U.S. Veterinary Market
Date:6/5/2008

ounting principles; trade buying patterns; the impact of legislation and regulatory compliance; risks and uncertainties associated with global operations and sales; and other risks and uncertainties, including those detailed from time to time in our periodic reports filed with the Securities and Exchange Commission, including our current reports on Form 8-K, quarterly reports on Form 10-Q and annual report on Form 10-K, particularly the discussion under the caption "Item 1A, Risk Factors" in our Annual Report on Form 10-K for the year ended December 31, 2007, which was filed with the Securities and Exchange Commission on February 29, 2008. The forward-looking statements in this press release are qualified by these risk factors. We assume no obligation to publicly update any forward-looking statements, whether as a result of new information, future developments or otherwise.

ProHeart(R) 6 is generally well tolerated. Do not use in sick, debilitated or underweight animals, animals with a history of weight loss, or within one month of vaccination. Use with caution in dogs with pre-existing allergic disease. A small percentage of dogs showed mild, transient swelling or itching at the injection site. While rare, allergic, digestive, hematological, or neurological reactions may occur. In addition, death has been reported. ProHeart 6 is available only through a restricted distribution program. Only veterinarians enrolled in this program can receive and administer ProHeart 6. In addition, ProHeart 6 must only be administered to clients whose owners have been advised of the risks of ProHeart 6 and sign an Owner Consent Form. To obtain additional information including a copy of the product labeling, visit the website at http://www.proheart6dvm.com or call 1-800-533-8536.


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SOURCE Fort Dodge Animal Health
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