美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CHOLESTYRAMINE LIGHT"
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
CHOLESTYRAMINE LIGHT 074558 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/PACKET No Yes 1996/08/15 1996/08/15 EPIC PHARMA LLC Prescription
CHOLESTYRAMINE LIGHT 074558 002 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 1996/08/15 1996/08/15 EPIC PHARMA LLC Prescription
CHOLESTYRAMINE LIGHT 074348 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/PACKET No No 1998/05/28 1998/05/28 TEVA Discontinued
CHOLESTYRAMINE LIGHT 074348 002 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 1998/05/28 1998/05/28 TEVA Discontinued
CHOLESTYRAMINE LIGHT 074555 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/PACKET No No 1998/09/30 1998/09/30 TEVA PHARMS Discontinued
CHOLESTYRAMINE LIGHT 074555 002 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 1998/09/30 1998/09/30 TEVA PHARMS Discontinued
CHOLESTYRAMINE LIGHT 077203 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/PACKET No No 2005/08/26 2005/08/26 PAR PHARM Prescription
CHOLESTYRAMINE LIGHT 077203 002 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 2005/08/26 2005/08/26 PAR PHARM Prescription
CHOLESTYRAMINE LIGHT 202902 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 2017/04/25 2017/04/25 ZYDUS PHARMS Prescription
CHOLESTYRAMINE LIGHT 209599 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/PACKET No No 2020/11/12 2020/11/12 TAGI Prescription
CHOLESTYRAMINE LIGHT 209599 002 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 2020/11/12 2020/11/12 TAGI Prescription
CHOLESTYRAMINE LIGHT 211799 001 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/PACKET No No 2021/10/19 2021/10/19 ALKEM LABS LTD Prescription
CHOLESTYRAMINE LIGHT 211799 002 ANDA CHOLESTYRAMINE POWDER;ORAL EQ 4GM RESIN/SCOOPFUL No No 2021/10/19 2021/10/19 ALKEM LABS LTD Prescription
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