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
55700-963-60	55700-963	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20220217	20260531	NDA AUTHORIZED GENERIC	NDA021908	Quality Care Products, LLC	LUBIPROSTONE	24 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (55700-963-60)
72189-607-60	72189-607	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20250116	N/A	NDA AUTHORIZED GENERIC	NDA021908	Direct Rx	LUBIPROSTONE	24 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)
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)
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)
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)
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)
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)
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)
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)
76420-907-01	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)
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)
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)
76420-906-60	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)