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）
检索条件:" 注册申请号=ANDA211763"
符合检索条件的记录共 18 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
62332-404-30 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)
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)
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)
62332-402-91 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)
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)
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)
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)
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