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）

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
71205-831-72	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)
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)
83008-001-60	83008-001	HUMAN PRESCRIPTION DRUG	Lubiprostone	lubiprostone	CAPSULE, GELATIN COATED	ORAL	20230314	20260831	NDA AUTHORIZED GENERIC	NDA021908	Quality Care Products, LLC	LUBIPROSTONE	24 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (83008-001-60)
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)
69339-162-17	69339-162	HUMAN PRESCRIPTION DRUG	LUBIPROSTONE	LUBIPROSTONE	CAPSULE, GELATIN COATED	ORAL	20221017	N/A	NDA AUTHORIZED GENERIC	NDA021908	Natco Pharma USA LLC	LUBIPROSTONE	8 ug/1	40 BLISTER PACK in 1 CARTON (69339-162-17) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (69339-162-98)
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)
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)
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)