美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ATOMOXETINE HYDROCHLORIDE"
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
ATOMOXETINE HYDROCHLORIDE 079017 001 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 18MG No No 2010/09/16 2010/09/17 ZYDUS PHARMS USA INC Prescription
ATOMOXETINE HYDROCHLORIDE 079017 002 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 2010/09/16 2010/09/17 ZYDUS PHARMS USA INC Prescription
ATOMOXETINE HYDROCHLORIDE 079017 003 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 40MG No No 2010/09/16 2010/09/17 ZYDUS PHARMS USA INC Prescription
ATOMOXETINE HYDROCHLORIDE 079017 004 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 60MG No No 2010/09/16 2010/09/17 ZYDUS PHARMS USA INC Prescription
ATOMOXETINE HYDROCHLORIDE 079017 005 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 80MG No No 2010/09/16 2010/09/17 ZYDUS PHARMS USA INC Prescription
ATOMOXETINE HYDROCHLORIDE 079017 006 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 100MG No No 2010/09/16 2010/09/17 ZYDUS PHARMS USA INC Prescription
ATOMOXETINE HYDROCHLORIDE 078940 002 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 18MG No 2012/05/11 (TA) ACTAVIS ELIZABETH None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 078940 003 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 25MG No 2012/05/11 (TA) ACTAVIS ELIZABETH None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 078940 004 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 40MG No 2012/05/11 (TA) ACTAVIS ELIZABETH None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 078940 005 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 60MG No 2012/05/11 (TA) ACTAVIS ELIZABETH None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 078940 006 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 80MG No 2012/05/11 (TA) ACTAVIS ELIZABETH None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 078940 007 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE;ORAL 100MG No 2012/05/11 (TA) ACTAVIS ELIZABETH None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 001 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 10MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 002 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 18MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 003 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 25MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 004 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 40MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 005 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 60MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 006 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 80MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079020 007 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 100MG No 2012/05/11 (TA) SUN PHARMA GLOBAL None (Tentative Approval)
ATOMOXETINE HYDROCHLORIDE 079021 001 ANDA ATOMOXETINE HYDROCHLORIDE CAPSULE; ORAL 10MG No 2012/05/11 (TA) MYLAN PHARMS INC None (Tentative Approval)
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