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"
符合检索条件的记录共 61 条，共 4 页，当前第 3 页 ，可点击列名称排序
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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
64764-240-60 64764-240 HUMAN PRESCRIPTION DRUG Amitiza lubiprostone CAPSULE, GELATIN COATED ORAL 20060131 20270331 NDA NDA021908 Takeda Pharmaceuticals America, Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (64764-240-60)
0254-3028-02 0254-3028 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20210101 N/A NDA AUTHORIZED GENERIC NDA021908 Par Health USA, LLC LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0254-3028-02)
76420-906-01 76420-906 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 8 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-01)
76420-906-30 76420-906 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 8 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-30)
76420-906-60 76420-906 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-60)
76420-906-90 76420-906 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 8 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-90)
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)
63304-352-60 63304-352 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230101 N/A NDA AUTHORIZED GENERIC NDA021908 Sun Pharmaceutical Industries, Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)
72189-607-60 72189-607 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20250116 N/A NDA AUTHORIZED GENERIC NDA021908 Direct Rx LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)
71205-831-67 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-67)
71205-831-72 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-72)
23635-508-60 23635-508 HUMAN PRESCRIPTION DRUG Amitiza lubiprostone CAPSULE, GELATIN COATED ORAL 20240401 N/A NDA NDA021908 SpecGx LLC LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (23635-508-60)
71205-831-78 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-78)
71205-831-90 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-90)
76420-907-01 76420-907 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 24 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-01)
76420-907-30 76420-907 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 24 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-30)
76420-907-60 76420-907 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-60)
76420-907-90 76420-907 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20250128 N/A NDA AUTHORIZED GENERIC NDA021908 Asclemed USA, Inc. LUBIPROSTONE 24 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-90)
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