FDA Requests Removal of Oxymorphone Hydrochloride for Risks Related to Abuse
June 9, 2017 - On June 8,the U.S. Food and Drug Administration (FDA) requested that Endo Pharmaceuticals remove its opioid pain medication, reformulated oxymorphone hydrochloride, from the market. After careful consideration, the agency is seeking removal based on its concern ...Leggi tutto