美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=THEO-DUR"
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
THEO-DUR 087995 001 ANDA THEOPHYLLINE CAPSULE, EXTENDED RELEASE;ORAL 200MG No No -- 1985/09/10 SCHERING Discontinued
THEO-DUR 088015 001 ANDA THEOPHYLLINE CAPSULE, EXTENDED RELEASE;ORAL 75MG No No -- 1985/09/10 SCHERING Discontinued
THEO-DUR 088016 001 ANDA THEOPHYLLINE CAPSULE, EXTENDED RELEASE;ORAL 125MG No No -- 1985/09/10 SCHERING Discontinued
THEO-DUR 088022 001 ANDA THEOPHYLLINE CAPSULE, EXTENDED RELEASE;ORAL 50MG No No -- 1985/09/10 SCHERING Discontinued
THEO-DUR 085328 001 ANDA THEOPHYLLINE TABLET, EXTENDED RELEASE;ORAL 100MG No No 1979/04/12 Approved Prior to Jan 1, 1982 SCHERING Discontinued
THEO-DUR 085328 002 ANDA THEOPHYLLINE TABLET, EXTENDED RELEASE;ORAL 300MG No No 1979/04/12 Approved Prior to Jan 1, 1982 SCHERING Discontinued
THEO-DUR 086998 001 ANDA THEOPHYLLINE TABLET, EXTENDED RELEASE;ORAL 200MG No No 1980/01/31 Approved Prior to Jan 1, 1982 SCHERING Discontinued
THEO-DUR 089131 001 ANDA THEOPHYLLINE TABLET, EXTENDED RELEASE;ORAL 450MG No No 1986/06/25 1986/06/25 SCHERING Discontinued
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