美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CALCIUM ACETATE"
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
CALCIUM ACETATE 077693 001 ANDA CALCIUM ACETATE TABLET;ORAL 667MG No No 2008/01/30 2008/01/30 HIKMA Discontinued
CALCIUM ACETATE 077728 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2008/02/26 2008/02/26 HIKMA Prescription
CALCIUM ACETATE 091561 001 ANDA CALCIUM ACETATE TABLET;ORAL 667MG No No 2011/04/13 2011/04/13 PADAGIS US Prescription
CALCIUM ACETATE 091312 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2012/06/01 2012/06/01 CHARTWELL RX Prescription
CALCIUM ACETATE 202420 001 ANDA CALCIUM ACETATE TABLET;ORAL 667MG No Yes 2013/02/05 2013/02/05 CHARTWELL MOLECULAR Prescription
CALCIUM ACETATE 203135 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No Yes 2013/02/07 2013/02/07 INVAGEN PHARMS Prescription
CALCIUM ACETATE 201658 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2014/10/06 2014/10/06 AMNEAL PHARMS Discontinued
CALCIUM ACETATE 202885 001 ANDA CALCIUM ACETATE TABLET;ORAL 667MG No No 2015/01/22 2015/01/22 HERITAGE PHARMS INC Prescription
CALCIUM ACETATE 202315 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2015/06/29 2015/06/29 HERITAGE PHARMS INC Prescription
CALCIUM ACETATE 202127 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2015/07/09 2015/07/09 LUPIN LTD Prescription
CALCIUM ACETATE 203179 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2015/10/26 2015/10/26 NOSTRUM LABS INC Prescription
CALCIUM ACETATE 203298 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2016/07/26 2016/07/26 LOTUS PHARM CO LTD Discontinued
CALCIUM ACETATE 211038 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2020/02/21 2020/02/21 SUVEN PHARMS Prescription
CALCIUM ACETATE 217205 001 ANDA CALCIUM ACETATE CAPSULE;ORAL 667MG No No 2023/03/13 2023/03/13 SQUARE PHARMS Prescription
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