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
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)
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)
71205-831-00 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-00)
71205-831-11 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 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-11)
71205-831-30 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 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-30)
71205-831-55 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-55)
71205-831-60 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 60 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-60)
71205-831-64 71205-831 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20231018 N/A NDA AUTHORIZED GENERIC NDA021908 Proficient Rx LP LUBIPROSTONE 8 ug/1 240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-831-64)
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)
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)
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)
0254-3029-02 0254-3029 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20210101 N/A NDA AUTHORIZED GENERIC NDA021908 Endo USA, Inc. LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0254-3029-02)
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)
23635-524-60 23635-524 HUMAN PRESCRIPTION DRUG Amitiza lubiprostone CAPSULE, GELATIN COATED ORAL 20240401 N/A NDA NDA021908 SPECGX LLC LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (23635-524-60)
80425-0354-2 80425-0354 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230816 N/A NDA AUTHORIZED GENERIC NDA021908 Advanced Rx Pharmacy of Tennessee, LLC LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (80425-0354-2)
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)
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