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Wyeth-Ayerst Low-Dose Premarin Filings Slated For 2000

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Executive Summary

Wyeth-Ayerst is planning to file for FDA approval of lower dose formulations of its conjugated estrogen product Premarin by the end of the year.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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