美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=VIVACTIL"
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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
VIVACTIL 016012 001 NDA PROTRIPTYLINE HYDROCHLORIDE TABLET;ORAL 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1967/09/27 Approved Prior to Jan 1, 1982 TEVA WOMENS Discontinued
VIVACTIL 016012 002 NDA PROTRIPTYLINE HYDROCHLORIDE TABLET;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1967/09/27 Approved Prior to Jan 1, 1982 TEVA WOMENS Discontinued
VIVACTIL 073644 001 ANDA PROTRIPTYLINE HYDROCHLORIDE TABLET;ORAL 5MG No No 1995/08/24 1995/08/24 CHARTWELL RX Discontinued
VIVACTIL 073645 001 ANDA PROTRIPTYLINE HYDROCHLORIDE TABLET;ORAL 10MG No No 1995/08/24 1995/08/24 CHARTWELL RX Discontinued
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