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
68012-002-13	68012-002	HUMAN PRESCRIPTION DRUG	Glumetza	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20060801	N/A	NDA	NDA021748	Santarus, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68012-002-13)
68012-003-16	68012-003	HUMAN PRESCRIPTION DRUG	Glumetza	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20080617	N/A	NDA	NDA021748	Santarus, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68012-003-16)
68682-018-90	68682-018	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20080617	N/A	NDA AUTHORIZED GENERIC	NDA021748	Oceanside Pharmaceuticals	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-018-90)
68012-004-50	68012-004	HUMAN PRESCRIPTION DRUG	Glumetza	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180320	N/A	NDA	NDA021748	Santarus, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68012-004-50)
68682-021-50	68682-021	HUMAN PRESCRIPTION DRUG	Metformin hydrochloride	metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180320	N/A	NDA AUTHORIZED GENERIC	NDA021748	Oceanside Pharmaceuticals	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-021-50)