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
71205-832-60	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	60 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-60)
71205-832-64	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	240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-64)
71205-832-67	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	270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-67)
71205-832-72	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	120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-72)
71205-832-78	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	180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-78)
71205-832-90	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	90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-90)
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)
69339-163-17	69339-163	HUMAN PRESCRIPTION DRUG	LUBIPROSTONE	LUBIPROSTONE	CAPSULE, GELATIN COATED	ORAL	20221017	N/A	NDA AUTHORIZED GENERIC	NDA021908	Natco Pharma USA LLC	LUBIPROSTONE	24 ug/1	40 BLISTER PACK in 1 CARTON (69339-163-17) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (69339-163-98)
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)
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)
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)