美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=AZACITIDINE"
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
AZACITIDINE 201537 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2013/09/16 2013/09/16 DR REDDYS Prescription
AZACITIDINE 204949 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2016/04/28 2016/04/28 MYLAN INSTITUTIONAL Discontinued
AZACITIDINE 208216 001 NDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2016/04/29 2016/04/29 ACTAVIS LLC Prescription
AZACITIDINE 207518 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2016/09/29 2016/09/29 SHILPA MEDICARE Prescription
AZACITIDINE 207234 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2017/06/23 2017/06/23 NATCO PHARMA LTD Prescription
AZACITIDINE 209540 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2018/05/04 2018/05/04 CIPLA Prescription
AZACITIDINE 207475 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2018/07/02 2018/07/02 ACCORD HLTHCARE Prescription
AZACITIDINE 210748 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2019/02/27 2019/02/27 LUPIN LTD Discontinued
AZACITIDINE 209337 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2020/06/08 2020/06/08 EUROHLTH INTL SARL Prescription
AZACITIDINE 212128 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2020/11/02 2020/11/02 MEITHEAL Prescription
AZACITIDINE 211549 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2022/02/03 2022/02/03 AMNEAL Prescription
AZACITIDINE 215066 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2022/12/30 2022/12/30 EUGIA PHARMA Prescription
AZACITIDINE 215905 001 ANDA AZACITIDINE POWDER;INTRAVENOUS, SUBCUTANEOUS 100MG/VIAL No No 2023/06/28 2023/06/28 JIANGSU HANSOH PHARM Prescription
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