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=ANDA210154"
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
70710-1033-8 70710-1033 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20220912 N/A ANDA ANDA210154 Zydus Pharmaceuticals USA Inc. LENALIDOMIDE 15 mg/1 21 CAPSULE in 1 BOTTLE (70710-1033-8)
70710-1031-7 70710-1031 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20220912 N/A ANDA ANDA210154 Zydus Pharmaceuticals USA Inc. LENALIDOMIDE 5 mg/1 28 CAPSULE in 1 BOTTLE (70710-1031-7)
70710-1034-1 70710-1034 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20230307 N/A ANDA ANDA210154 Zydus Pharmaceuticals USA Inc. LENALIDOMIDE 20 mg/1 100 CAPSULE in 1 BOTTLE (70710-1034-1)
70710-1034-8 70710-1034 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20230307 N/A ANDA ANDA210154 Zydus Pharmaceuticals USA Inc. LENALIDOMIDE 20 mg/1 21 CAPSULE in 1 BOTTLE (70710-1034-8)
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