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
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)
0254-3029-02 0254-3029 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20210101 N/A NDA AUTHORIZED GENERIC NDA021908 Par Health USA, LLC LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0254-3029-02)
51407-744-60 51407-744 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230123 N/A NDA AUTHORIZED GENERIC NDA021908 Golden State Medical Supply, Inc. LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (51407-744-60)
51407-745-60 51407-745 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230123 N/A NDA AUTHORIZED GENERIC NDA021908 Golden State Medical Supply, Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (51407-745-60)
0406-6408-60 0406-6408 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20240501 N/A NDA AUTHORIZED GENERIC NDA021908 SpecGx LLC LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0406-6408-60)
0406-6424-60 0406-6424 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20240501 N/A NDA AUTHORIZED GENERIC NDA021908 SpecGx LLC LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0406-6424-60)
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)
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)
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)
43598-163-60 43598-163 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230101 N/A NDA AUTHORIZED GENERIC NDA021908 Dr. Reddy's Laboratories Inc. LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-163-60)
43598-168-60 43598-168 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230101 N/A NDA AUTHORIZED GENERIC NDA021908 Dr. Reddy's Laboratories Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-168-60)
82804-001-30 82804-001 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230824 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 30 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-30)
82804-001-60 82804-001 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230824 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-60)
82804-001-90 82804-001 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20230824 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 24 ug/1 90 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-90)
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