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=ANDA210402"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
69238-1626-3 69238-1626 HUMAN PRESCRIPTION DRUG DIMETHYL FUMARATE DIMETHYL FUMARATE KIT 20200928 N/A ANDA ANDA210402 Amneal Pharmaceuticals NY LLC 1 KIT in 1 KIT (69238-1626-3) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
69238-1319-6 69238-1319 HUMAN PRESCRIPTION DRUG Dimethyl Fumarate Dimethyl Fumarate CAPSULE, DELAYED RELEASE ORAL 20200928 N/A ANDA ANDA210402 Amneal Pharmaceuticals NY LLC DIMETHYL FUMARATE 240 mg/1 1 BOTTLE in 1 CARTON (69238-1319-6) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE
69238-1318-4 69238-1318 HUMAN PRESCRIPTION DRUG Dimethyl Fumarate Dimethyl Fumarate CAPSULE, DELAYED RELEASE ORAL 20200928 N/A ANDA ANDA210402 Amneal Pharmaceuticals NY LLC DIMETHYL FUMARATE 120 mg/1 1 BOTTLE in 1 CARTON (69238-1318-4) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
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