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K-V Pharmaceutical Company Notified by New York Stock Exchange of Non-Compliance With Continued Listing Standards
Date:8/2/2010

aterial adverse effect, if any, on its revenue, assets and liquidity and capital resources, as more fully described in Note 20 – "Subsequent Events" of the Notes to the Consolidated Financial Statements in the Form 10-Q;

(7) changes in the current and future business environment, including interest rates and capital and consumer spending;

(8) the difficulty of predicting FDA approvals, including timing, and that any period of exclusivity may not be realized;

(9) the possibility of not obtaining FDA approvals or delay in obtaining FDA approvals, including with respect to Gestiva™, as well as the number of preterm births for which Gestiva™ may be prescribed, its safety profile and side effects profile;

(10) acceptance of and demand for the Company's new pharmaceutical products or current products upon their return to the marketplace;

(11) the introduction and impact of competitive products and pricing, including as a result of so-called authorized generic drugs;

(12) new product development and launch, including the possibility that any product launch may be delayed;

(13) reliance on key strategic acquisitions;

(14) the availability of raw materials and/or products manufactured for the Company under contract manufacturing agreements with third parties;

(15) the regulatory environment, including regulatory agency and judicial actions and changes in applicable laws or regulations;

(16) fluctuations in revenues;

(17) the difficulty of predicting international regulatory approvals, including timing;

(18) the difficulty of predicting the pattern of invent
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SOURCE K-V Pharmaceutical Company
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