美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=AZATHIOPRINE"
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
AZATHIOPRINE 071056 001 ANDA AZATHIOPRINE SODIUM Injectable; Injection EQ 100MG BASE/VIAL No -- QUAD PHARMS Discontinued
AZATHIOPRINE SODIUM 074419 001 ANDA AZATHIOPRINE SODIUM INJECTABLE;INJECTION EQ 100MG BASE/VIAL No Yes 1995/03/31 1995/03/31 WEST-WARD PHARMS INT Prescription
AZATHIOPRINE 074069 001 ANDA AZATHIOPRINE TABLET;ORAL 50MG No No 1996/02/16 1996/02/16 AMNEAL PHARMS LLC Prescription
AZATHIOPRINE 075568 001 ANDA AZATHIOPRINE TABLET;ORAL 50MG No No 1999/12/13 1999/12/13 MYLAN Prescription
AZATHIOPRINE 077621 001 ANDA AZATHIOPRINE TABLET;ORAL 50MG No No 2007/03/15 2007/03/15 ZYDUS PHARMS USA Prescription
AZATHIOPRINE 077621 002 ANDA AZATHIOPRINE TABLET;ORAL 25MG No No 2007/03/15 2008/09/05 ZYDUS PHARMS USA Prescription
AZATHIOPRINE 077621 003 ANDA AZATHIOPRINE TABLET;ORAL 75MG No No 2007/03/15 2008/09/05 ZYDUS PHARMS USA Prescription
AZATHIOPRINE 077621 004 ANDA AZATHIOPRINE TABLET;ORAL 100MG No No 2007/03/15 2008/09/05 ZYDUS PHARMS USA Prescription
AZATHIOPRINE 208687 001 ANDA AZATHIOPRINE TABLET;ORAL 25MG No No 2020/03/27 2020/03/27 ALKEM LABS LTD Prescription
AZATHIOPRINE 208687 002 ANDA AZATHIOPRINE TABLET;ORAL 50MG No No 2020/03/27 2020/03/27 ALKEM LABS LTD Prescription
AZATHIOPRINE 208687 003 ANDA AZATHIOPRINE TABLET;ORAL 75MG No No 2020/03/27 2020/03/27 ALKEM LABS LTD Prescription
AZATHIOPRINE 208687 004 ANDA AZATHIOPRINE TABLET;ORAL 100MG No No 2020/03/27 2020/03/27 ALKEM LABS LTD Prescription
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