Fed Regist. 2003 May 22;68(99):27937-9.
This interim final rule amends the Federal opioid treatment program regulations by adding buprenorphine and buprenorphine combination products to the list of approved opioid treatment medications that may be used in federally certified and registered opioid treatment programs. The Food and Drug Administration (FDA) recently approved Subutex[reg] (buprenorphine) and Suboxone[reg] (buprenorphine in fixed combination with naloxone) for the treatment of opiate dependence. These two products will join methadone and ORLAAM[reg] as medications that may be used in opioid treatment programs for the maintenance and detoxification treatment of opioid dependence. Opioid treatment programs that choose to use these new products in the treatment of opioid dependence will adhere to the same Federal treatment standards established for methadone and ORLAAM[reg]. The Secretary invites public comments on this action.
本暂行最终规则修订了联邦阿片类药物治疗项目法规,将丁丙诺啡及丁丙诺啡复方产品添加到经联邦认证和注册的阿片类药物治疗项目中可使用的获批阿片类治疗药物清单中。美国食品药品监督管理局(FDA)最近批准了舒倍生(丁丙诺啡)和舒泊西(丁丙诺啡与纳洛酮的固定复方制剂)用于治疗阿片类药物依赖。这两种产品将与美沙酮和环丙甲羟二氢吗啡酮一同作为可用于阿片类药物治疗项目中维持治疗和脱毒治疗阿片类药物依赖的药物。选择使用这些新产品治疗阿片类药物依赖的阿片类药物治疗项目将遵守为美沙酮和环丙甲羟二氢吗啡酮制定的相同联邦治疗标准。部长邀请公众对该行动发表评论。