美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ALBUTEROL"
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 208804 001 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 2MG BASE No No 2018/05/21 2018/05/21 AMNEAL PHARMS CO Prescription
ALBUTEROL SULFATE 208804 002 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 4MG BASE No No 2018/05/21 2018/05/21 AMNEAL PHARMS CO Prescription
ALBUTEROL SULFATE 207046 001 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 2MG BASE No No 2018/06/29 2018/06/29 APPCO PHARMA LLC Prescription
ALBUTEROL SULFATE 207046 002 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 4MG BASE No No 2018/06/29 2018/06/29 APPCO PHARMA LLC Prescription
ALBUTEROL SULFATE 211397 001 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 2MG BASE No No 2018/10/26 2018/10/26 VIRTUS PHARM Prescription
ALBUTEROL SULFATE 211397 002 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 4MG BASE No No 2018/10/26 2018/10/26 VIRTUS PHARM Prescription
LEVALBUTEROL HYDROCHLORIDE 207820 001 ANDA LEVALBUTEROL HYDROCHLORIDE SOLUTION;INHALATION EQ 0.0103% BASE No No 2018/11/05 2018/11/05 SUN PHARM Prescription
LEVALBUTEROL HYDROCHLORIDE 207820 002 ANDA LEVALBUTEROL HYDROCHLORIDE SOLUTION;INHALATION EQ 0.021% BASE No No 2018/11/05 2018/11/05 SUN PHARM Prescription
LEVALBUTEROL HYDROCHLORIDE 207820 003 ANDA LEVALBUTEROL HYDROCHLORIDE SOLUTION;INHALATION EQ 0.042% BASE No No 2018/11/05 2018/11/05 SUN PHARM Prescription
ALBUTEROL SULFATE 210948 001 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 2MG BASE No No 2019/03/15 2019/03/15 ARISE Prescription
ALBUTEROL SULFATE 210948 002 ANDA ALBUTEROL SULFATE TABLET;ORAL EQ 4MG BASE No No 2019/03/15 2019/03/15 ARISE Prescription
ALBUTEROL SULFATE 212197 001 ANDA ALBUTEROL SULFATE SYRUP;ORAL EQ 2MG BASE/5ML No No 2019/09/06 2019/09/06 QUAGEN Prescription
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