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China’s State FDA Approves Aoxing R&D License For Anti-Opioid Addiction Drug

This article was originally published in PharmAsia News

Executive Summary

SHANGHAI - China's State Food and Drug Administration approved a research and development license Nov. 20 for Aoxing Pharmaceutical's opioid combo tablet buprenorphine/naloxone tailored to fight the growing problem of opioid dependence in China
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