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
60687-816-32	60687-816	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20251201	N/A	ANDA	ANDA209920	American Health Packaging	LUBIPROSTONE	8 ug/1	20 BLISTER PACK in 1 CARTON (60687-816-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-816-33)
0480-3479-06	0480-3479	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20230103	N/A	ANDA	ANDA209920	Teva Pharmaceuticals, Inc.	LUBIPROSTONE	8 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (0480-3479-06)
72189-410-60	72189-410	HUMAN PRESCRIPTION DRUG	Amitza	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20230112	N/A	ANDA	ANDA209920	Direct_Rx	LUBIPROSTONE	8 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-410-60)
60687-827-32	60687-827	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20251126	N/A	ANDA	ANDA209920	American Health Packaging	LUBIPROSTONE	24 ug/1	20 BLISTER PACK in 1 CARTON (60687-827-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-827-33)
0480-4138-06	0480-4138	HUMAN PRESCRIPTION DRUG	Lubiprostone	Lubiprostone	CAPSULE, GELATIN COATED	ORAL	20230103	N/A	ANDA	ANDA209920	Teva Pharmaceuticals, Inc.	LUBIPROSTONE	24 ug/1	60 CAPSULE, GELATIN COATED in 1 BOTTLE (0480-4138-06)