美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=PARAPLATIN"
符合检索条件的记录共 7 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
PARAPLATIN 019880 001 NDA CARBOPLATIN INJECTABLE;INJECTION 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/03/03 1989/03/03 CORDEN PHARMA Discontinued
PARAPLATIN 019880 002 NDA CARBOPLATIN INJECTABLE;INJECTION 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/03/03 1989/03/03 CORDEN PHARMA Discontinued
PARAPLATIN 019880 003 NDA CARBOPLATIN INJECTABLE;INJECTION 450MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1989/03/03 1989/03/03 CORDEN PHARMA Discontinued
PARAPLATIN 020452 001 NDA CARBOPLATIN INJECTABLE;INTRAVENOUS 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2003/07/14 2003/07/14 CORDENPHARMA Discontinued
PARAPLATIN 020452 002 NDA CARBOPLATIN INJECTABLE;INTRAVENOUS 150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2003/07/14 2003/07/14 CORDENPHARMA Discontinued
PARAPLATIN 020452 003 NDA CARBOPLATIN INJECTABLE;INTRAVENOUS 450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2003/07/14 2003/07/14 CORDENPHARMA Discontinued
PARAPLATIN 020452 004 NDA CARBOPLATIN INJECTABLE;INTRAVENOUS 600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2003/07/14 2004/01/15 CORDENPHARMA Discontinued
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