美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE"
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
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 076867 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2006/12/21 2006/12/21 FOSUN PHARMA Discontinued
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 077063 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2007/04/13 (TA) 2007/12/31 WATSON LABS TEVA Discontinued
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 076724 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2007/12/31 2007/12/31 TEVA PHARMS Discontinued
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 076749 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No Yes 2007/12/31 2007/12/31 NEPHRON Prescription
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 077063 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2007/12/31 2007/12/31 WATSON LABS TEVA Discontinued
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 077117 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2007/12/31 2007/12/31 APOTEX INC Discontinued
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 077559 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2007/12/31 2007/12/31 CIPLA Prescription
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 202496 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2012/10/01 2012/10/01 RITEDOSE CORP Prescription
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 207875 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2017/08/07 2017/08/07 SUN PHARM Prescription
ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE 206532 001 ANDA ALBUTEROL SULFATE; IPRATROPIUM BROMIDE SOLUTION;INHALATION EQ 0.083% BASE;0.017% No No 2020/07/09 2020/07/08 LUOXIN AUROVITAS Discontinued
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