美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SODIUM BUTABARBITAL"
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 083484 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 15MG No No 1973/09/25 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
SODIUM BUTABARBITAL 083524 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 16.2MG No No 1974/01/15 Approved Prior to Jan 1, 1982 MARSHALL PHARMA Discontinued
SODIUM BUTABARBITAL 083858 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 32.4MG No No 1974/03/14 Approved Prior to Jan 1, 1982 MARSHALL PHARMA Discontinued
SODIUM BUTABARBITAL 084040 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 30MG No No 1974/05/31 Approved Prior to Jan 1, 1982 IVAX SUB TEVA PHARMS Discontinued
SODIUM BUTABARBITAL 085418 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 15MG No No 1977/08/15 Approved Prior to Jan 1, 1982 HIKMA PHARMS Discontinued
SODIUM BUTABARBITAL 085432 001 ANDA BUTABARBITAL SODIUM TABLET;ORAL 30MG No No 1977/12/20 Approved Prior to Jan 1, 1982 HIKMA PHARMS Discontinued
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
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