美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=NDA018934"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
62135-321-90 62135-321 HUMAN PRESCRIPTION DRUG Methyldopa Methyldopa TABLET, FILM COATED ORAL 20221122 N/A NDA NDA018934 Chartwell RX, LLC METHYLDOPA 250 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (62135-321-90)
62135-322-18 62135-322 HUMAN PRESCRIPTION DRUG Methyldopa Methyldopa TABLET, FILM COATED ORAL 20221122 N/A NDA NDA018934 Chartwell RX, LLC METHYLDOPA 500 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (62135-322-18)
62135-322-90 62135-322 HUMAN PRESCRIPTION DRUG Methyldopa Methyldopa TABLET, FILM COATED ORAL 20221122 N/A NDA NDA018934 Chartwell RX, LLC METHYLDOPA 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (62135-322-90)
62135-321-18 62135-321 HUMAN PRESCRIPTION DRUG Methyldopa Methyldopa TABLET, FILM COATED ORAL 20221122 N/A NDA NDA018934 Chartwell RX, LLC METHYLDOPA 250 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (62135-321-18)
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