美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ALDOMET"
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
ALDOMET 013400 001 NDA METHYLDOPA TABLET;ORAL 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1962/12/20 Approved Prior to Jan 1, 1982 MERCK Discontinued
ALDOMET 013400 002 NDA METHYLDOPA TABLET;ORAL 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1962/12/20 Approved Prior to Jan 1, 1982 MERCK Discontinued
ALDOMET 013400 003 NDA METHYLDOPA TABLET;ORAL 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1962/12/20 Approved Prior to Jan 1, 1982 MERCK Discontinued
ALDOMET 013401 001 NDA METHYLDOPATE HYDROCHLORIDE INJECTABLE;INJECTION 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1962/12/20 Approved Prior to Jan 1, 1982 MERCK Discontinued
ALDOMET 018389 001 NDA METHYLDOPA SUSPENSION;ORAL 250MG/5ML No No 1981/08/28 Approved Prior to Jan 1, 1982 MERCK Discontinued
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