美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DIETHYLPROPION HYDROCHLORIDE"
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
DIETHYLPROPION HYDROCHLORIDE 085544 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 UCB INC Discontinued
DIETHYLPROPION HYDROCHLORIDE 085741 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 1979/08/15 Approved Prior to Jan 1, 1982 WATSON LABS Discontinued
DIETHYLPROPION HYDROCHLORIDE 088267 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 1983/08/25 1983/08/25 CHARTWELL RX Discontinued
DIETHYLPROPION HYDROCHLORIDE 088268 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 1983/08/25 1983/08/25 CHARTWELL RX Discontinued
DIETHYLPROPION HYDROCHLORIDE 088642 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 1984/09/20 1984/09/20 TEVA Discontinued
DIETHYLPROPION HYDROCHLORIDE 085916 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 1994/09/16 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
DIETHYLPROPION HYDROCHLORIDE 040828 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 2008/11/05 2008/11/05 EPIC PHARMA LLC Discontinued
DIETHYLPROPION HYDROCHLORIDE 201212 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No No 2010/12/22 2010/12/22 AVANTHI INC Prescription
DIETHYLPROPION HYDROCHLORIDE 200177 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET;ORAL 25MG No Yes 2011/07/18 2011/07/18 LANNETT CO INC Prescription
DIETHYLPROPION HYDROCHLORIDE 091680 001 ANDA DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 75MG No Yes 2011/10/24 2011/10/24 LANNETT CO INC Prescription
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