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
70518-4032-0	70518-4032	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20240305	N/A	ANDA	ANDA212682	REMEDYREPACK INC.	NEBIVOLOL	5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4032-0)
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)
71335-2516-1	71335-2516	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20241024	N/A	ANDA	ANDA212682	Bryant Ranch Prepack	NEBIVOLOL	5 mg/1	30 TABLET in 1 BOTTLE (71335-2516-1)
71335-2516-2	71335-2516	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20241024	N/A	ANDA	ANDA212682	Bryant Ranch Prepack	NEBIVOLOL	5 mg/1	90 TABLET in 1 BOTTLE (71335-2516-2)
63629-9589-1	63629-9589	HUMAN PRESCRIPTION DRUG	NEBIVOLOL	nebivolol	TABLET	ORAL	20221201	N/A	ANDA	ANDA212682	Bryant Ranch Prepack	NEBIVOLOL	5 mg/1	90 TABLET in 1 BOTTLE (63629-9589-1)
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)