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
49884-257-01	49884-257	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	19881114	N/A	ANDA	ANDA071839	Par Pharmaceutical, Inc.	MINOXIDIL	10 mg/1	100 TABLET in 1 BOTTLE (49884-257-01)
49884-257-05	49884-257	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	19881114	N/A	ANDA	ANDA071839	Par Pharmaceutical, Inc.	MINOXIDIL	10 mg/1	500 TABLET in 1 BOTTLE (49884-257-05)
63629-2230-1	63629-2230	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20210322	N/A	ANDA	ANDA071839	Bryant Ranch Prepack	MINOXIDIL	10 mg/1	100 TABLET in 1 BOTTLE (63629-2230-1)
63629-2231-1	63629-2231	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20210322	N/A	ANDA	ANDA071839	Bryant Ranch Prepack	MINOXIDIL	10 mg/1	500 TABLET in 1 BOTTLE (63629-2231-1)
63629-9299-1	63629-9299	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20220606	N/A	ANDA	ANDA071839	Bryant Ranch Prepack	MINOXIDIL	10 mg/1	100 TABLET in 1 BOTTLE (63629-9299-1)
63629-9620-1	63629-9620	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20230327	N/A	ANDA	ANDA071839	Bryant Ranch Prepack	MINOXIDIL	10 mg/1	100 TABLET in 1 BOTTLE (63629-9620-1)
63629-9620-2	63629-9620	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20230327	N/A	ANDA	ANDA071839	Bryant Ranch Prepack	MINOXIDIL	10 mg/1	30 TABLET in 1 BOTTLE (63629-9620-2)
72162-1490-5	72162-1490	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20230421	N/A	ANDA	ANDA071839	Bryant Ranch Prepack	MINOXIDIL	10 mg/1	500 TABLET in 1 BOTTLE (72162-1490-5)
68084-205-01	68084-205	HUMAN PRESCRIPTION DRUG	Minoxidil	Minoxidil	TABLET	ORAL	20070705	N/A	ANDA	ANDA071839	American Health Packaging	MINOXIDIL	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-205-01) / 1 TABLET in 1 BLISTER PACK (68084-205-11)