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
68382-734-77	68382-734	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Pharmaceuticals USA Inc.	NADOLOL	80 mg/1	10 BLISTER PACK in 1 CARTON (68382-734-77) / 1 TABLET in 1 BLISTER PACK (68382-734-30)
71335-0697-1	71335-0697	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20180219	N/A	ANDA	ANDA207761	Bryant Ranch Prepack	NADOLOL	80 mg/1	30 TABLET in 1 BOTTLE (71335-0697-1)
71335-0697-2	71335-0697	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20180219	N/A	ANDA	ANDA207761	Bryant Ranch Prepack	NADOLOL	80 mg/1	28 TABLET in 1 BOTTLE (71335-0697-2)
71335-0697-3	71335-0697	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20180219	N/A	ANDA	ANDA207761	Bryant Ranch Prepack	NADOLOL	80 mg/1	90 TABLET in 1 BOTTLE (71335-0697-3)
68382-732-10	68382-732	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Pharmaceuticals USA Inc.	NADOLOL	20 mg/1	1000 TABLET in 1 BOTTLE (68382-732-10)
68382-732-16	68382-732	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Pharmaceuticals USA Inc.	NADOLOL	20 mg/1	90 TABLET in 1 BOTTLE (68382-732-16)
68382-732-77	68382-732	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Pharmaceuticals USA Inc.	NADOLOL	20 mg/1	10 BLISTER PACK in 1 CARTON (68382-732-77) / 1 TABLET in 1 BLISTER PACK (68382-732-30)