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
68462-209-01	68462-209	HUMAN PRESCRIPTION DRUG	Moexipril Hydrochloride	Moexipril Hydrochloride	TABLET, FILM COATED	ORAL	20101231	N/A	ANDA	ANDA090416	Glenmark Pharmaceuticals Inc., USA	MOEXIPRIL HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-209-01)
68462-209-10	68462-209	HUMAN PRESCRIPTION DRUG	Moexipril Hydrochloride	Moexipril Hydrochloride	TABLET, FILM COATED	ORAL	20101231	N/A	ANDA	ANDA090416	Glenmark Pharmaceuticals Inc., USA	MOEXIPRIL HYDROCHLORIDE	7.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-209-10)
68462-209-90	68462-209	HUMAN PRESCRIPTION DRUG	Moexipril Hydrochloride	Moexipril Hydrochloride	TABLET, FILM COATED	ORAL	20101231	N/A	ANDA	ANDA090416	Glenmark Pharmaceuticals Inc., USA	MOEXIPRIL HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-209-90)
68462-208-90	68462-208	HUMAN PRESCRIPTION DRUG	Moexipril Hydrochloride	Moexipril Hydrochloride	TABLET, FILM COATED	ORAL	20101231	N/A	ANDA	ANDA090416	Glenmark Pharmaceuticals Inc., USA	MOEXIPRIL HYDROCHLORIDE	15 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-208-90)
68462-208-10	68462-208	HUMAN PRESCRIPTION DRUG	Moexipril Hydrochloride	Moexipril Hydrochloride	TABLET, FILM COATED	ORAL	20101231	N/A	ANDA	ANDA090416	Glenmark Pharmaceuticals Inc., USA	MOEXIPRIL HYDROCHLORIDE	15 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-208-10)
68462-208-01	68462-208	HUMAN PRESCRIPTION DRUG	Moexipril Hydrochloride	Moexipril Hydrochloride	TABLET, FILM COATED	ORAL	20101231	N/A	ANDA	ANDA090416	Glenmark Pharmaceuticals Inc., USA	MOEXIPRIL HYDROCHLORIDE	15 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-208-01)