美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SUBOXONE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
SUBOXONE 020733 001 NDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE TABLET;SUBLINGUAL EQ 2MG BASE;EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2002/10/08 2002/10/08 INDIVIOR INC Discontinued
SUBOXONE 020733 002 NDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE TABLET;SUBLINGUAL EQ 8MG BASE;EQ 2MG BASE Yes No 2002/10/08 2002/10/08 INDIVIOR INC Discontinued
SUBOXONE 022410 001 NDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 2MG BASE;EQ 0.5MG BASE Yes No 2010/08/30 2010/08/30 INDIVIOR INC Prescription
SUBOXONE 022410 002 NDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 8MG BASE;EQ 2MG BASE Yes No 2010/08/30 2010/08/30 INDIVIOR INC Prescription
SUBOXONE 022410 003 NDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 4MG BASE;EQ 1MG BASE Yes No 2010/08/30 2012/08/10 INDIVIOR INC Prescription
SUBOXONE 022410 004 NDA BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE FILM;BUCCAL, SUBLINGUAL EQ 12MG BASE;EQ 3MG BASE Yes Yes 2010/08/30 2012/08/10 INDIVIOR INC Prescription
药品名称,活性成分,申请号搜索 高级检索
©2006-2019 DrugFuture->U.S. FDA Drugs Database