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
72578-004-10	72578-004	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20190228	N/A	ANDA	ANDA090961	Viona Pharmaceuticals Inc	MEMANTINE HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE (72578-004-10)
72578-004-14	72578-004	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20190228	N/A	ANDA	ANDA090961	Viona Pharmaceuticals Inc	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET in 1 BOTTLE (72578-004-14)
72578-004-77	72578-004	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20190228	N/A	ANDA	ANDA090961	Viona Pharmaceuticals Inc	MEMANTINE HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (72578-004-77) / 10 TABLET in 1 BLISTER PACK (72578-004-30)
72162-2004-5	72162-2004	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20240206	N/A	ANDA	ANDA090961	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE (72162-2004-5)
72162-2004-6	72162-2004	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20240206	N/A	ANDA	ANDA090961	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET in 1 BOTTLE (72162-2004-6)
72162-2003-5	72162-2003	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET	ORAL	20240206	N/A	ANDA	ANDA090961	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (72162-2003-5)