美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=TEGRETOL"
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
TEGRETOL 016608 001 NDA CARBAMAZEPINE TABLET;ORAL 200MG Yes Yes 1968/03/11 Approved Prior to Jan 1, 1982 NOVARTIS Prescription
TEGRETOL 018281 001 NDA CARBAMAZEPINE TABLET, CHEWABLE;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1981/12/14 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
TEGRETOL 018927 001 NDA CARBAMAZEPINE SUSPENSION;ORAL 100MG/5ML Yes Yes 1987/12/18 1987/12/18 NOVARTIS Prescription
TEGRETOL-XR 020234 001 NDA CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 100MG Yes No 1996/03/25 1996/03/25 NOVARTIS Prescription
TEGRETOL-XR 020234 002 NDA CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 200MG Yes No 1996/03/25 1996/03/25 NOVARTIS Prescription
TEGRETOL-XR 020234 003 NDA CARBAMAZEPINE TABLET, EXTENDED RELEASE;ORAL 400MG Yes Yes 1996/03/25 1996/03/25 NOVARTIS Prescription
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