美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=NEUPRO"
符合检索条件的记录共 6 条
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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
NEUPRO 021829 001 NDA ROTIGOTINE FILM, EXTENDED RELEASE;TRANSDERMAL 2MG/24HR Yes Yes 2007/05/09 2007/05/09 UCB INC Prescription
NEUPRO 021829 002 NDA ROTIGOTINE FILM, EXTENDED RELEASE;TRANSDERMAL 4MG/24HR Yes No 2007/05/09 2007/05/09 UCB INC Prescription
NEUPRO 021829 003 NDA ROTIGOTINE FILM, EXTENDED RELEASE;TRANSDERMAL 6MG/24HR Yes No 2007/05/09 2007/05/09 UCB INC Prescription
NEUPRO 021829 004 NDA ROTIGOTINE FILM, EXTENDED RELEASE;TRANSDERMAL 1MG/24HR Yes No 2007/05/09 2012/04/02 UCB INC Prescription
NEUPRO 021829 005 NDA ROTIGOTINE FILM, EXTENDED RELEASE;TRANSDERMAL 3MG/24HR Yes No 2007/05/09 2012/04/02 UCB INC Prescription
NEUPRO 021829 006 NDA ROTIGOTINE FILM, EXTENDED RELEASE;TRANSDERMAL 8MG/24HR Yes No 2007/05/09 2012/04/02 UCB INC Prescription
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