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
65862-459-60	65862-459	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-459-60)
65862-459-71	65862-459	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	8 mg/1	7000 TABLET, FILM COATED in 1 BOTTLE (65862-459-71)
65862-459-99	65862-459	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	8 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-459-99)
65862-458-99	65862-458	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	4 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-458-99)
65862-458-60	65862-458	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-458-60)
65862-460-49	65862-460	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	12 mg/1	4000 TABLET, FILM COATED in 1 BOTTLE (65862-460-49)
65862-458-19	65862-458	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	4 mg/1	10000 TABLET, FILM COATED in 1 BOTTLE (65862-458-19)
65862-460-60	65862-460	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	12 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-460-60)
65862-460-99	65862-460	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Aurobindo Pharma Limited	GALANTAMINE HYDROBROMIDE	12 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-460-99)
68084-729-21	68084-729	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090957	American Health Packaging	GALANTAMINE HYDROBROMIDE	4 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-729-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-729-11)
57237-050-60	57237-050	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Rising Pharma Holdings, Inc.	GALANTAMINE HYDROBROMIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (57237-050-60)
57237-051-60	57237-051	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Rising Pharma Holdings, Inc.	GALANTAMINE HYDROBROMIDE	12 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (57237-051-60)
57237-049-60	57237-049	HUMAN PRESCRIPTION DRUG	Galantamine	Galantamine	TABLET, FILM COATED	ORAL	20110329	N/A	ANDA	ANDA090957	Rising Pharma Holdings, Inc.	GALANTAMINE HYDROBROMIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (57237-049-60)