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
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)
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)
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)
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)
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)
69339-163-17	69339-163	HUMAN PRESCRIPTION DRUG	LUBIPROSTONE	LUBIPROSTONE	CAPSULE	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 in 1 BLISTER PACK (69339-163-98)
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)
43598-168-60	43598-168	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20230101	N/A	NDA AUTHORIZED GENERIC	NDA021908	Dr. Reddy's Laboratories Inc.	LUBIPROSTONE	24 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-168-60)