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
63629-9589-2	63629-9589	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20221201	N/A	ANDA	ANDA212682	Bryant Ranch Prepack	NEBIVOLOL	5 mg/1	30 TABLET in 1 BOTTLE (63629-9589-2)
0904-7498-04	0904-7498	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20250224	N/A	ANDA	ANDA212682	Major Pharmaceuticals	NEBIVOLOL	5 mg/1	30 BLISTER PACK in 1 CARTON (0904-7498-04) / 1 TABLET in 1 BLISTER PACK
43547-525-03	43547-525	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20220214	N/A	ANDA	ANDA212682	Solco Healthcare US, LLC	NEBIVOLOL	5 mg/1	30 TABLET in 1 BOTTLE (43547-525-03)
43547-525-09	43547-525	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20220214	N/A	ANDA	ANDA212682	Solco Healthcare US, LLC	NEBIVOLOL	5 mg/1	90 TABLET in 1 BOTTLE (43547-525-09)
43547-525-50	43547-525	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20220214	N/A	ANDA	ANDA212682	Solco Healthcare US, LLC	NEBIVOLOL	5 mg/1	500 TABLET in 1 BOTTLE (43547-525-50)
72189-592-60	72189-592	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241030	N/A	ANDA	ANDA212682	Direct_Rx	NEBIVOLOL	20 mg/1	60 TABLET in 1 BOTTLE (72189-592-60)
71335-2443-1	71335-2443	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebibolol	TABLET	ORAL	20240815	N/A	ANDA	ANDA212682	Bryant Ranch Prepack	NEBIVOLOL	10 mg/1	30 TABLET in 1 BOTTLE (71335-2443-1)
71335-2443-2	71335-2443	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebibolol	TABLET	ORAL	20240815	N/A	ANDA	ANDA212682	Bryant Ranch Prepack	NEBIVOLOL	10 mg/1	90 TABLET in 1 BOTTLE (71335-2443-2)