美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=NORMODYNE"
符合检索条件的记录共 5 条
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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
NORMODYNE 018686 001 NDA LABETALOL HYDROCHLORIDE INJECTABLE;INJECTION 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/08/01 1984/08/01 SCHERING Discontinued
NORMODYNE 018687 001 NDA LABETALOL HYDROCHLORIDE TABLET;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/08/01 1987/08/31 SCHERING Discontinued
NORMODYNE 018687 002 NDA LABETALOL HYDROCHLORIDE TABLET;ORAL 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/08/01 1984/08/01 SCHERING Discontinued
NORMODYNE 018687 003 NDA LABETALOL HYDROCHLORIDE TABLET;ORAL 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/08/01 1984/08/01 SCHERING Discontinued
NORMODYNE 018687 004 NDA LABETALOL HYDROCHLORIDE TABLET;ORAL 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1984/08/01 1984/08/01 SCHERING Discontinued
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