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=ANDA218640"
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
72603-288-01 72603-288 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE ORAL 20250701 N/A ANDA ANDA218640 Northstar Rx LLC LUBIPROSTONE .008 mg/1 60 CAPSULE in 1 BOTTLE (72603-288-01)
72603-289-01 72603-289 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE ORAL 20250701 N/A ANDA ANDA218640 Northstar Rx LLC LUBIPROSTONE .024 mg/1 60 CAPSULE in 1 BOTTLE (72603-289-01)
31722-404-60 31722-404 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE ORAL 20250527 N/A ANDA ANDA218640 Camber Pharmaceuticals, Inc. LUBIPROSTONE .024 mg/1 60 CAPSULE in 1 BOTTLE (31722-404-60)
31722-403-60 31722-403 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE ORAL 20250527 N/A ANDA ANDA218640 Camber Pharmaceuticals, Inc. LUBIPROSTONE .008 mg/1 60 CAPSULE in 1 BOTTLE (31722-403-60)
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