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
61442-192-05	61442-192	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20250622	N/A	ANDA	ANDA212947	Carlsbad Technology, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (61442-192-05)
61442-192-60	61442-192	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20250622	N/A	ANDA	ANDA212947	Carlsbad Technology, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (61442-192-60)
61442-193-05	61442-193	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20250622	N/A	ANDA	ANDA212947	Carlsbad Technology, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (61442-193-05)
61442-193-60	61442-193	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20250622	N/A	ANDA	ANDA212947	Carlsbad Technology, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (61442-193-60)