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=ANDA210382"
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
51407-442-14 51407-442 HUMAN PRESCRIPTION DRUG dimethyl fumarate dimethyl fumarate CAPSULE, DELAYED RELEASE ORAL 20210420 N/A ANDA ANDA210382 Golden State Medical Supply, Inc. DIMETHYL FUMARATE 120 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51407-442-14)
24979-127-02 24979-127 HUMAN PRESCRIPTION DRUG dimethyl fumarate dimethyl fumarate CAPSULE, DELAYED RELEASE ORAL 20201201 N/A ANDA ANDA210382 TWi Pharmaceuticals, Inc. DIMETHYL FUMARATE 120 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (24979-127-02)
24979-127-21 24979-127 HUMAN PRESCRIPTION DRUG dimethyl fumarate dimethyl fumarate CAPSULE, DELAYED RELEASE ORAL 20201201 N/A ANDA ANDA210382 TWi Pharmaceuticals, Inc. DIMETHYL FUMARATE 120 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (24979-127-21)
51407-441-60 51407-441 HUMAN PRESCRIPTION DRUG dimethyl fumarate dimethyl fumarate CAPSULE, DELAYED RELEASE ORAL 20210105 N/A ANDA ANDA210382 Golden State Medical Supply, Inc. DIMETHYL FUMARATE 240 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51407-441-60)
24979-128-02 24979-128 HUMAN PRESCRIPTION DRUG dimethyl fumarate dimethyl fumarate CAPSULE, DELAYED RELEASE ORAL 20201201 N/A ANDA ANDA210382 TWi Pharmaceuticals, Inc. DIMETHYL FUMARATE 240 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (24979-128-02)
24979-128-04 24979-128 HUMAN PRESCRIPTION DRUG dimethyl fumarate dimethyl fumarate CAPSULE, DELAYED RELEASE ORAL 20201201 N/A ANDA ANDA210382 TWi Pharmaceuticals, Inc. DIMETHYL FUMARATE 240 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (24979-128-04)
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