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
47335-305-18	47335-305	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180522	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-18)
47335-305-83	47335-305	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180522	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-83)
47335-305-88	47335-305	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180522	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-88)
47335-306-18	47335-306	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180522	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-18)
47335-306-81	47335-306	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190722	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-81)
47335-306-83	47335-306	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180522	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-83)
47335-306-88	47335-306	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180522	N/A	ANDA	ANDA202917	Sun Pharmaceutical Industries, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-88)