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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
TENUATE 011722 002 NDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1959/08/06 Approved Prior to Jan 1, 1982 NOSTRUM LABS INC Discontinued
TENUATE DOSPAN 012546 001 NDA DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1960/11/17 Approved Prior to Jan 1, 1982 NOSTRUM LABS INC Discontinued
TENUATE 017668 001 NDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 1975/03/20 Approved Prior to Jan 1, 1982 SANOFI AVENTIS US Discontinued
TENUATE 017669 001 NDA DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 75MG No No 1975/03/20 Approved Prior to Jan 1, 1982 SANOFI AVENTIS US Discontinued
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