美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=INFUGEM"
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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
INFUGEM 208313 001 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1200MG BASE/120ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 002 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1300MG BASE/130ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 003 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1400MG BASE/140ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 004 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1500MG BASE/150ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 005 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1600MG BASE/160ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 006 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1700MG BASE/170ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 007 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1800MG BASE/180ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 008 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 1900MG BASE/190ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 009 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 2000MG BASE/200ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
INFUGEM 208313 010 NDA GEMCITABINE HYDROCHLORIDE SOLUTION;INTRAVENOUS EQ 2200MG BASE/220ML (EQ 10MG BASE/ML) Yes No 2018/07/16 2018/07/16 SUN PHARM Discontinued
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