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Prawo i regulacje · 10/03/2020

FDA Approves Cenobamate for New Drug Application, DEA to Place in Schedule V

The U.S. Food and Drug Administration (FDA) approved a new drug application for XCOPRI (cenobamate) tablets on November 21, 2019, leading to a recommendation by the Department of Health and Human Services to place cenobamate in schedule V of the Controlled Substances Act (CSA).

Source: Federal Register — Justice DepartmentOpen original release →