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
52605-071-10	52605-071	HUMAN PRESCRIPTION DRUG	memantine hydrochloride	memantine hydrochloride	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA210587	POLYGEN PHARMACEUTICALS INC.	MEMANTINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (52605-071-10)
52605-071-13	52605-071	HUMAN PRESCRIPTION DRUG	memantine hydrochloride	memantine hydrochloride	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA210587	POLYGEN PHARMACEUTICALS INC.	MEMANTINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (52605-071-13)
52605-071-16	52605-071	HUMAN PRESCRIPTION DRUG	memantine hydrochloride	memantine hydrochloride	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA210587	POLYGEN PHARMACEUTICALS INC.	MEMANTINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (52605-071-16)
52605-072-10	52605-072	HUMAN PRESCRIPTION DRUG	Memantine hydrochloride	Memantine hydrochloride	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA210587	POLYGEN PHARMACEUTICALS INC.	MEMANTINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (52605-072-10)
52605-072-13	52605-072	HUMAN PRESCRIPTION DRUG	Memantine hydrochloride	Memantine hydrochloride	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA210587	POLYGEN PHARMACEUTICALS INC.	MEMANTINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (52605-072-13)
52605-072-16	52605-072	HUMAN PRESCRIPTION DRUG	Memantine hydrochloride	Memantine hydrochloride	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA210587	POLYGEN PHARMACEUTICALS INC.	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (52605-072-16)