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
0527-1221-05	0527-1221	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20161110	N/A	ANDA	ANDA207236	Lannett Company, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (0527-1221-05)
0527-1221-06	0527-1221	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20161110	N/A	ANDA	ANDA207236	Lannett Company, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (0527-1221-06)
0527-1221-10	0527-1221	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20161110	N/A	ANDA	ANDA207236	Lannett Company, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0527-1221-10)
0527-1222-05	0527-1222	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20161110	N/A	ANDA	ANDA207236	Lannett Company, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (0527-1222-05)
0527-1222-06	0527-1222	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20161110	N/A	ANDA	ANDA207236	Lannett Company, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (0527-1222-06)
0527-1222-10	0527-1222	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20161110	N/A	ANDA	ANDA207236	Lannett Company, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0527-1222-10)