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
47335-321-08	47335-321	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-321-08)
47335-321-18	47335-321	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-321-18)
47335-321-86	47335-321	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-321-86)
47335-321-88	47335-321	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-321-88)
47335-322-08	47335-322	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-322-08)
47335-322-13	47335-322	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-322-13)
47335-322-18	47335-322	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-322-18)
47335-322-83	47335-322	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-322-83)
47335-322-86	47335-322	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-322-86)
47335-322-88	47335-322	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20150711	N/A	ANDA	ANDA090058	Sun Pharmaceutical Industries, Inc.	MEMANTINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-322-88)
71335-1908-1	71335-1908	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20210715	N/A	ANDA	ANDA090058	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1908-1)
71335-1908-2	71335-1908	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20210715	N/A	ANDA	ANDA090058	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1908-2)
71335-1908-3	71335-1908	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20210715	N/A	ANDA	ANDA090058	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1908-3)
71335-1908-4	71335-1908	HUMAN PRESCRIPTION DRUG	Memantine Hydrochloride	Memantine Hydrochloride	TABLET, FILM COATED	ORAL	20210715	N/A	ANDA	ANDA090058	Bryant Ranch Prepack	MEMANTINE HYDROCHLORIDE	10 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1908-4)