美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=A-POXIDE"
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
A-POXIDE 085447 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 5MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
A-POXIDE 085447 002 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 10MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
A-POXIDE 085447 003 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 25MG No No -- Approved Prior to Jan 1, 1982 ABBOTT Discontinued
A-POXIDE 085513 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 25MG No No 1977/06/30 Approved Prior to Jan 1, 1982 ABBOTT Discontinued
A-POXIDE 085517 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 5MG No No 1977/07/01 Approved Prior to Jan 1, 1982 ABBOTT Discontinued
A-POXIDE 085518 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 10MG No No 1977/07/01 Approved Prior to Jan 1, 1982 ABBOTT Discontinued
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