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
50090-0771-3	50090-0771	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20141128	N/A	ANDA	ANDA075967	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET in 1 BOTTLE (50090-0771-3)
57664-397-51	57664-397	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET in 1 BOTTLE (57664-397-51)
57664-397-53	57664-397	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET in 1 BOTTLE (57664-397-53)
57664-397-58	57664-397	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET in 1 BOTTLE (57664-397-58)
57664-397-59	57664-397	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET in 1 BOTTLE (57664-397-59)
57664-435-51	57664-435	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET in 1 BOTTLE (57664-435-51)
57664-435-53	57664-435	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	500 TABLET in 1 BOTTLE (57664-435-53)
57664-435-58	57664-435	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	1000 TABLET in 1 BOTTLE (57664-435-58)
57664-435-59	57664-435	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	90 TABLET in 1 BOTTLE (57664-435-59)
57664-474-51	57664-474	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET in 1 BOTTLE (57664-474-51)
57664-474-53	57664-474	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET in 1 BOTTLE (57664-474-53)
57664-474-58	57664-474	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET in 1 BOTTLE (57664-474-58)
57664-474-59	57664-474	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET	ORAL	20020129	N/A	ANDA	ANDA075967	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET in 1 BOTTLE (57664-474-59)