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)
70518-2139-0	70518-2139	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20190610	N/A	ANDA	ANDA207761	REMEDYREPACK INC.	NADOLOL	40 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-2139-0)
70771-1089-1	70771-1089	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Lifesciences Limited	NADOLOL	20 mg/1	100 TABLET in 1 BOTTLE (70771-1089-1)
70771-1089-4	70771-1089	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Lifesciences Limited	NADOLOL	20 mg/1	10 BLISTER PACK in 1 CARTON (70771-1089-4) / 1 TABLET in 1 BLISTER PACK (70771-1089-2)
70771-1089-9	70771-1089	HUMAN PRESCRIPTION DRUG	Nadolol	Nadolol	TABLET	ORAL	20170808	N/A	ANDA	ANDA207761	Zydus Lifesciences Limited	NADOLOL	20 mg/1	90 TABLET in 1 BOTTLE (70771-1089-9)