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
71209-059-11	71209-059	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE (71209-059-11)
71209-060-01	71209-060	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (71209-060-01)
71209-060-04	71209-060	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	10 mg/1	90 TABLET in 1 BOTTLE (71209-060-04)
71209-060-05	71209-060	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (71209-060-05)
71209-060-11	71209-060	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE (71209-060-11)
71209-061-01	71209-061	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (71209-061-01)
71209-061-04	71209-061	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE (71209-061-04)
71209-061-05	71209-061	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (71209-061-05)
71209-061-11	71209-061	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE (71209-061-11)
71209-058-04	71209-058	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	90 TABLET in 1 BOTTLE (71209-058-04)
71209-058-05	71209-058	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (71209-058-05)
71209-058-11	71209-058	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20181016	N/A	ANDA	ANDA208717	Cadila Pharmaceuticals Limited	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	1000 TABLET in 1 BOTTLE (71209-058-11)
72162-2416-3	72162-2416	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (72162-2416-3)
72162-2416-9	72162-2416	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE (72162-2416-9)
72162-2417-3	72162-2417	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (72162-2417-3)
72162-2417-9	72162-2417	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	5 mg/1	90 TABLET in 1 BOTTLE (72162-2417-9)
72162-2414-3	72162-2414	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (72162-2414-3)
72162-2414-9	72162-2414	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	10 mg/1	90 TABLET in 1 BOTTLE (72162-2414-9)
72162-2415-3	72162-2415	HUMAN PRESCRIPTION DRUG	Nebivolol	Nebivolol	TABLET	ORAL	20241031	N/A	ANDA	ANDA208717	Bryant Ranch Prepack	NEBIVOLOL HYDROCHLORIDE	2.5 mg/1	30 TABLET in 1 BOTTLE (72162-2415-3)