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=ANDA210305"
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
69097-322-89 69097-322 HUMAN PRESCRIPTION DRUG DIMETHYL FUMARATE DIMETHYL FUMARATE CAPSULE, DELAYED RELEASE ORAL 20200924 N/A ANDA ANDA210305 Cipla USA Inc. DIMETHYL FUMARATE 120 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (69097-322-89) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
69097-323-03 69097-323 HUMAN PRESCRIPTION DRUG DIMETHYL FUMARATE DIMETHYL FUMARATE CAPSULE, DELAYED RELEASE ORAL 20200924 N/A ANDA ANDA210305 Cipla USA Inc. DIMETHYL FUMARATE 240 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (69097-323-03) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
69097-552-03 69097-552 HUMAN PRESCRIPTION DRUG DIMETHYL FUMARATE DIMETHYL FUMARATE KIT 20200924 N/A ANDA ANDA210305 Cipla USA Inc. 1 KIT in 1 KIT (69097-552-03) * 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC * 46 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
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