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
71205-834-00 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)
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)
83008-001-60 83008-001 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230314 N/A NDA AUTHORIZED GENERIC NDA021908 Quality Care Products, LLC LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (83008-001-60)
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)
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)
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)
63304-351-60 63304-351 HUMAN PRESCRIPTION DRUG Lubiprostone lubiprostone CAPSULE, GELATIN COATED ORAL 20230101 N/A NDA AUTHORIZED GENERIC NDA021908 Sun Pharmaceutical Industries, Inc. LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-351-60)
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)
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)
64764-080-60 64764-080 HUMAN PRESCRIPTION DRUG Amitiza lubiprostone CAPSULE, GELATIN COATED ORAL 20080429 20250930 NDA NDA021908 Takeda Pharmaceuticals America, Inc. LUBIPROSTONE 8 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (64764-080-60)
55700-963-60 55700-963 HUMAN PRESCRIPTION DRUG Lubiprostone Lubiprostone CAPSULE, GELATIN COATED ORAL 20220217 N/A NDA AUTHORIZED GENERIC NDA021908 Quality Care Products, LLC LUBIPROSTONE 24 ug/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (55700-963-60)
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