美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CELEXA"
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
CELEXA 020822 001 NDA CITALOPRAM HYDROBROMIDE TABLET;ORAL EQ 10MG BASE Yes No 1998/07/17 2000/04/27 ABBVIE Prescription
CELEXA 020822 002 NDA CITALOPRAM HYDROBROMIDE TABLET;ORAL EQ 20MG BASE Yes No 1998/07/17 1998/07/17 ABBVIE Prescription
CELEXA 020822 003 NDA CITALOPRAM HYDROBROMIDE TABLET;ORAL EQ 40MG BASE Yes Yes 1998/07/17 1998/07/17 ABBVIE Prescription
CELEXA 020822 004 NDA CITALOPRAM HYDROBROMIDE TABLET;ORAL EQ 60MG BASE No No 1998/07/17 1998/07/17 ABBVIE Discontinued
CELEXA 021046 001 NDA CITALOPRAM HYDROBROMIDE SOLUTION;ORAL EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1999/12/22 1999/12/22 FOREST LABS Discontinued
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