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
62332-402-91	62332-402	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	20 mg/1	1000 TABLET in 1 BOTTLE (62332-402-91)
62332-403-30	62332-403	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	40 mg/1	30 TABLET in 1 BOTTLE (62332-403-30)
62332-403-31	62332-403	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	40 mg/1	100 TABLET in 1 BOTTLE (62332-403-31)
62332-403-91	62332-403	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	40 mg/1	1000 TABLET in 1 BOTTLE (62332-403-91)
62332-404-30	62332-404	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	80 mg/1	30 TABLET in 1 BOTTLE (62332-404-30)
62332-404-31	62332-404	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	80 mg/1	100 TABLET in 1 BOTTLE (62332-404-31)
62332-404-91	62332-404	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	80 mg/1	1000 TABLET in 1 BOTTLE (62332-404-91)
46708-402-30	46708-402	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	20 mg/1	30 TABLET in 1 BOTTLE (46708-402-30)
46708-402-31	46708-402	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	20 mg/1	100 TABLET in 1 BOTTLE (46708-402-31)
46708-402-91	46708-402	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	20 mg/1	1000 TABLET in 1 BOTTLE (46708-402-91)
46708-403-30	46708-403	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	40 mg/1	30 TABLET in 1 BOTTLE (46708-403-30)
46708-403-31	46708-403	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	40 mg/1	100 TABLET in 1 BOTTLE (46708-403-31)
46708-403-91	46708-403	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	40 mg/1	1000 TABLET in 1 BOTTLE (46708-403-91)
46708-404-30	46708-404	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	80 mg/1	30 TABLET in 1 BOTTLE (46708-404-30)
46708-404-31	46708-404	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	80 mg/1	100 TABLET in 1 BOTTLE (46708-404-31)
46708-404-91	46708-404	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Limited	NADOLOL	80 mg/1	1000 TABLET in 1 BOTTLE (46708-404-91)
62332-402-31	62332-402	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	20 mg/1	100 TABLET in 1 BOTTLE (62332-402-31)
62332-402-30	62332-402	HUMAN PRESCRIPTION DRUG	NADOLOL	NADOLOL	TABLET	ORAL	20230608	N/A	ANDA	ANDA211763	Alembic Pharmaceuticals Inc.	NADOLOL	20 mg/1	30 TABLET in 1 BOTTLE (62332-402-30)