美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SECONAL SODIUM"
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
SECONAL SODIUM 086530 001 ANDA SECOBARBITAL SODIUM SUPPOSITORY;RECTAL 30MG No No -- Approved Prior to Jan 1, 1982 LILLY Discontinued
SECONAL SODIUM 086530 002 ANDA SECOBARBITAL SODIUM SUPPOSITORY;RECTAL 60MG No No -- Approved Prior to Jan 1, 1982 LILLY Discontinued
SECONAL SODIUM 086530 003 ANDA SECOBARBITAL SODIUM SUPPOSITORY;RECTAL 120MG No No -- Approved Prior to Jan 1, 1982 LILLY Discontinued
SECONAL SODIUM 086530 004 ANDA SECOBARBITAL SODIUM SUPPOSITORY;RECTAL 200MG No No -- Approved Prior to Jan 1, 1982 LILLY Discontinued
SECONAL SODIUM 007392 002 NDA SECOBARBITAL SODIUM INJECTABLE;INJECTION 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1950/07/19 Approved Prior to Jan 1, 1982 LILLY Discontinued
SECONAL SODIUM 086101 001 ANDA SECOBARBITAL SODIUM CAPSULE;ORAL 50MG No No 1983/10/03 1983/10/03 VALEANT PHARMS NORTH Discontinued
SECONAL SODIUM 086101 002 ANDA SECOBARBITAL SODIUM CAPSULE;ORAL 100MG No No 1983/10/03 1983/10/03 VALEANT PHARMS NORTH Discontinued
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