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
68462-615-01	68462-615	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (68462-615-01)
68462-615-11	68462-615	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	10 BLISTER PACK in 1 CARTON (68462-615-11) / 10 TABLET in 1 BLISTER PACK
68462-615-30	68462-615	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	30 TABLET in 1 BOTTLE (68462-615-30)
68462-616-01	68462-616	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (68462-616-01)
68462-616-11	68462-616	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (68462-616-11) / 10 TABLET in 1 BLISTER PACK
68462-616-30	68462-616	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (68462-616-30)
68462-617-01	68462-617	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (68462-617-01)
68462-617-11	68462-617	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (68462-617-11) / 10 TABLET in 1 BLISTER PACK
68462-617-30	68462-617	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (68462-617-30)
68462-618-01	68462-618	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (68462-618-01)
68462-618-11	68462-618	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (68462-618-11) / 10 TABLET in 1 BLISTER PACK
68462-618-30	68462-618	HUMAN PRESCRIPTION DRUG	nebivolol	nebivolol hydrochloride	TABLET	ORAL	20170525	N/A	ANDA	ANDA203821	Glenmark Pharmaceuticals Inc., USA	NEBIVOLOL HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (68462-618-30)