美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DESONIDE"
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
DESONIDE 202161 001 ANDA DESONIDE LOTION;TOPICAL 0.05% No No 2014/10/31 2014/10/31 TARO Prescription
BUDESONIDE 204548 001 ANDA BUDESONIDE SUSPENSION;INHALATION 1MG/2ML No No 2016/03/08 2016/03/08 TEVA PHARMS USA Prescription
BUDESONIDE 206623 001 ANDA BUDESONIDE CAPSULE, DELAYED RELEASE;ORAL 3MG No No 2016/04/08 2016/04/08 DR REDDYS LABS SA Prescription
BUDESONIDE 206724 001 ANDA BUDESONIDE CAPSULE, DELAYED RELEASE;ORAL 3MG No No 2016/11/23 2016/11/23 NATCO Discontinued
DESONIDE 208836 001 ANDA DESONIDE OINTMENT;TOPICAL 0.05% No No 2017/03/27 2017/03/27 HIKMA Discontinued
BUDESONIDE 207367 001 ANDA BUDESONIDE CAPSULE, DELAYED RELEASE;ORAL 3MG No No 2017/04/07 2017/04/07 RISING Prescription
BUDESONIDE 206134 001 ANDA BUDESONIDE CAPSULE, DELAYED RELEASE;ORAL 3MG No No 2017/05/04 2017/05/04 ZYDUS PHARMS Prescription
DESONIDE 209729 001 ANDA DESONIDE CREAM;TOPICAL 0.05% No No 2017/07/24 2017/07/24 GLENMARK SPECLT Prescription
BUDESONIDE 206200 001 ANDA BUDESONIDE CAPSULE, DELAYED RELEASE;ORAL 3MG No No 2017/07/31 2017/07/31 AMNEAL PHARMS Prescription
DESONIDE 209996 001 ANDA DESONIDE OINTMENT;TOPICAL 0.05% No No 2017/09/15 2017/09/15 GLENMARK PHARMS LTD Prescription
DESONIDE 209494 001 ANDA DESONIDE LOTION;TOPICAL 0.05% No No 2017/09/26 2017/09/26 GLENMARK SPECLT Prescription
DESONIDE 207855 001 ANDA DESONIDE LOTION;TOPICAL 0.05% No No 2017/09/28 2017/09/28 PAI HOLDINGS PHARM Discontinued
BUDESONIDE 209041 001 ANDA BUDESONIDE CAPSULE, DELAYED RELEASE;ORAL 3MG No No 2017/09/28 2017/09/28 SCIECURE PHARMA INC Discontinued
BUDESONIDE 205710 001 ANDA BUDESONIDE SUSPENSION;INHALATION 0.25MG/2ML No No 2017/11/16 2017/11/16 CIPLA Prescription
BUDESONIDE 205710 002 ANDA BUDESONIDE SUSPENSION;INHALATION 0.5MG/2ML No No 2017/11/16 2017/11/16 CIPLA Prescription
BUDESONIDE 205710 003 ANDA BUDESONIDE SUSPENSION;INHALATION 1MG/2ML No No 2017/11/16 2017/11/16 CIPLA Prescription
BUDESONIDE 205457 001 ANDA BUDESONIDE TABLET, EXTENDED RELEASE;ORAL 9MG No No 2018/07/03 2018/07/03 ACTAVIS LABS FL INC Prescription
BUDESONIDE 210897 001 ANDA BUDESONIDE SUSPENSION;INHALATION 0.5MG/2ML No No 2018/11/09 2018/11/09 LUPIN Prescription
DESONIDE 210998 001 ANDA DESONIDE OINTMENT;TOPICAL 0.05% No No 2019/01/30 2019/01/30 ENCUBE ETHICALS Prescription
DESONIDE 212002 001 ANDA DESONIDE OINTMENT;TOPICAL 0.05% No No 2019/03/12 2019/03/12 PAI HOLDINGS PHARM Discontinued
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