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
49884-256-01	49884-256	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	19881114	N/A	ANDA	ANDA071826	Par Pharmaceutical, Inc.	MINOXIDIL	2.5 mg/1	100 TABLET in 1 BOTTLE (49884-256-01)
63629-2232-1	63629-2232	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20210322	N/A	ANDA	ANDA071826	Bryant Ranch Prepack	MINOXIDIL	2.5 mg/1	100 TABLET in 1 BOTTLE (63629-2232-1)
63629-9433-1	63629-9433	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20221017	N/A	ANDA	ANDA071826	Bryant Ranch Prepack	MINOXIDIL	2.5 mg/1	30 TABLET in 1 BOTTLE (63629-9433-1)
68788-8273-3	68788-8273	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20221013	N/A	ANDA	ANDA071826	Preferred Pharmaceuticals Inc.	MINOXIDIL	2.5 mg/1	30 TABLET in 1 BOTTLE (68788-8273-3)
72162-1489-1	72162-1489	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20231006	N/A	ANDA	ANDA071826	Bryant Ranch Prepack	MINOXIDIL	2.5 mg/1	100 TABLET in 1 BOTTLE (72162-1489-1)
68084-204-01	68084-204	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20070705	N/A	ANDA	ANDA071826	American Health Packaging	MINOXIDIL	2.5 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-204-01) / 1 TABLET in 1 BLISTER PACK (68084-204-11)