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
70710-1035-1 70710-1035 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20220912 N/A ANDA ANDA210154 Zydus Pharmaceuticals USA Inc. LENALIDOMIDE 25 mg/1 100 CAPSULE in 1 BOTTLE (70710-1035-1)
70710-1035-8 70710-1035 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20220912 N/A ANDA ANDA210154 Zydus Pharmaceuticals USA Inc. LENALIDOMIDE 25 mg/1 21 CAPSULE in 1 BOTTLE (70710-1035-8)
70771-1679-1 70771-1679 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20220912 N/A ANDA ANDA210154 Zydus Lifesciences Limited LENALIDOMIDE 15 mg/1 100 CAPSULE in 1 BOTTLE (70771-1679-1)
70771-1679-8 70771-1679 HUMAN PRESCRIPTION DRUG LENALIDOMIDE LENALIDOMIDE CAPSULE ORAL 20220912 N/A ANDA ANDA210154 Zydus Lifesciences Limited LENALIDOMIDE 15 mg/1 21 CAPSULE in 1 BOTTLE (70771-1679-8)
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