美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ESOMEPRAZOLE SODIUM"
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
ESOMEPRAZOLE SODIUM 200882 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 20MG BASE/VIAL No No 2013/03/18 2013/03/18 SUN PHARM Discontinued
ESOMEPRAZOLE SODIUM 200882 002 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No No 2013/03/18 2013/03/18 SUN PHARM Discontinued
ESOMEPRAZOLE SODIUM 205379 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No No 2015/09/25 2015/09/25 ACCORD HLTHCARE Discontinued
ESOMEPRAZOLE SODIUM 204657 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 20MG BASE/VIAL No No 2016/08/10 2016/08/10 EUGIA PHARMA Discontinued
ESOMEPRAZOLE SODIUM 204657 002 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No No 2016/08/10 2016/08/10 EUGIA PHARMA Prescription
ESOMEPRAZOLE SODIUM 207181 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No No 2017/03/06 2017/03/06 DEVA HOLDING AS Prescription
ESOMEPRAZOLE SODIUM 202686 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 20MG BASE/VIAL No No 2017/05/17 2017/05/17 MYLAN Discontinued
ESOMEPRAZOLE SODIUM 202686 002 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No No 2017/05/17 2017/05/17 MYLAN Discontinued
ESOMEPRAZOLE SODIUM 203349 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 20MG BASE/VIAL No Yes 2020/04/01 2020/04/01 GLAND PHARMA LTD Prescription
ESOMEPRAZOLE SODIUM 203349 002 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No No 2020/04/01 2020/04/01 GLAND PHARMA LTD Prescription
ESOMEPRAZOLE SODIUM 215732 001 ANDA ESOMEPRAZOLE SODIUM INJECTABLE;INTRAVENOUS EQ 40MG BASE/VIAL No Yes 2022/02/10 2022/02/10 SLATE RUN PHARMA Prescription
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