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FDA PREMARIN BIOEQUIVALENCE STANDARDS SHOULD BE KEPT, KIBBE TELLS HOUSE OVERSIGHT CMTE.; AGENCY SHOULD LIMIT EFFORTS BY INNOVATOR TO DELAY GENERICS

Executive Summary

FDA should stand by its 1991 decision on bioequivalence standards for Wyeth-Ayerst's Premarin, Arthur Kibbe, PhD, Wilkes University, told the House Commerce/Oversight Subcommittee June 19.
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