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
29300-399-01	29300-399	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210811	N/A	ANDA	ANDA213359	Unichem Pharmaceuticals (USA), Inc.	METFORMIN HYDROCHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-399-01)
29300-399-05	29300-399	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210811	N/A	ANDA	ANDA213359	Unichem Pharmaceuticals (USA), Inc.	METFORMIN HYDROCHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-399-05)
29300-389-01	29300-389	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210811	N/A	ANDA	ANDA213359	Unichem Pharmaceuticals (USA), Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-389-01)
29300-389-05	29300-389	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210811	N/A	ANDA	ANDA213359	Unichem Pharmaceuticals (USA), Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-389-05)
29300-389-10	29300-389	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210811	N/A	ANDA	ANDA213359	Unichem Pharmaceuticals (USA), Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-389-10)
29300-389-19	29300-389	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20210811	N/A	ANDA	ANDA213359	Unichem Pharmaceuticals (USA), Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-389-19)