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
51407-906-60	51407-906	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20240415	N/A	ANDA	ANDA077604	Golden State Medical Supply, Inc.	GALANTAMINE HYDROBROMIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (51407-906-60)
70436-004-06	70436-004	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20170802	N/A	ANDA	ANDA077604	Slate Run Pharmaceuticals, LLC	GALANTAMINE HYDROBROMIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70436-004-06)
70436-006-06	70436-006	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20170802	N/A	ANDA	ANDA077604	Slate Run Pharmaceuticals, LLC	GALANTAMINE HYDROBROMIDE	12 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70436-006-06)
51407-908-60	51407-908	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20240415	N/A	ANDA	ANDA077604	Golden State Medical Supply, Inc.	GALANTAMINE HYDROBROMIDE	12 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (51407-908-60)
24979-723-04	24979-723	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA077604	Upsher-Smith Laboratories, LLC	GALANTAMINE HYDROBROMIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (24979-723-04)
24979-724-04	24979-724	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA077604	Upsher-Smith Laboratories, LLC	GALANTAMINE HYDROBROMIDE	12 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (24979-724-04)
51407-907-60	51407-907	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20240415	N/A	ANDA	ANDA077604	Golden State Medical Supply, Inc.	GALANTAMINE HYDROBROMIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (51407-907-60)
24979-722-04	24979-722	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20240306	N/A	ANDA	ANDA077604	Upsher-Smith Laboratories, LLC	GALANTAMINE HYDROBROMIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (24979-722-04)
70436-005-06	70436-005	HUMAN PRESCRIPTION DRUG	Galantamine	galantamine	TABLET, FILM COATED	ORAL	20170802	N/A	ANDA	ANDA077604	Slate Run Pharmaceuticals, LLC	GALANTAMINE HYDROBROMIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70436-005-06)