美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=BUTABARB"
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
SODIUM BUTABARBITAL 085866 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 30MG No No 1978/07/20 Approved Prior to Jan 1, 1982 LANNETT Discontinued
SODIUM BUTABARBITAL 085881 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 100MG No No 1978/07/20 Approved Prior to Jan 1, 1982 LANNETT Discontinued
SODIUM BUTABARBITAL 085849 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 15MG No No 1978/08/21 Approved Prior to Jan 1, 1982 LANNETT Discontinued
BUTABARBITAL SODIUM 085383 001 ANDA BUTABARBITAL SODIUM ELIXIR;ORAL 30MG/5ML No No 1979/02/26 Approved Prior to Jan 1, 1982 WOCKHARDT Discontinued
BUTABARBITAL SODIUM 085934 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 30MG No No 1994/09/16 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
BUTABARBITAL SODIUM 085938 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 15MG No No 1994/09/16 Approved Prior to Jan 1, 1982 SANDOZ Discontinued
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