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
42571-333-01	42571-333	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-333-01)
42571-333-05	42571-333	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-333-05)
42571-333-60	42571-333	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-333-60)
42571-333-90	42571-333	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-333-90)
42571-334-01	42571-334	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-01)
42571-334-05	42571-334	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-05)
42571-334-60	42571-334	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-60)
42571-334-90	42571-334	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230301	N/A	ANDA	ANDA212448	Micro Labs Limited	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-90)