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=NDA021908"
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
71205-832-00 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-00)
71205-832-11 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-11)
71205-832-30 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-30)
71205-832-55 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-55)
71205-832-60 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-60)
71205-832-64 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-64)
71205-832-67 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-67)
71205-832-72 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-72)
71205-832-78 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-78)
71205-832-90 71205-832 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-90)
71205-834-00 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-00)
71205-834-11 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-11)
71205-834-30 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-30)
71205-834-55 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-55)
71205-834-60 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-60)
71205-834-64 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-64)
71205-834-67 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-67)
71205-834-72 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-72)
71205-834-78 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-78)
71205-834-90 71205-834 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230818 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-90)
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