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=ANDA203455"
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
72162-2233-1 72162-2233 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20240126 N/A ANDA ANDA203455 Bryant Ranch Prepack NADOLOL 40 mg/1 100 TABLET in 1 BOTTLE (72162-2233-1)
72162-2234-1 72162-2234 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20240126 N/A ANDA ANDA203455 Bryant Ranch Prepack NADOLOL 20 mg/1 100 TABLET in 1 BOTTLE (72162-2234-1)
68001-317-00 68001-317 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20170131 N/A ANDA ANDA203455 BluePoint Laboratories NADOLOL 20 mg/1 100 TABLET in 1 BOTTLE (68001-317-00)
68001-318-00 68001-318 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20170131 N/A ANDA ANDA203455 BluePoint Laboratories NADOLOL 40 mg/1 100 TABLET in 1 BOTTLE (68001-318-00)
60687-302-25 60687-302 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20170522 N/A ANDA ANDA203455 American Health Packaging NADOLOL 20 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-302-25) / 1 TABLET in 1 BLISTER PACK (60687-302-95)
60687-313-25 60687-313 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20170613 N/A ANDA ANDA203455 American Health Packaging NADOLOL 40 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-313-25) / 1 TABLET in 1 BLISTER PACK (60687-313-95)
68001-319-00 68001-319 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20170131 N/A ANDA ANDA203455 BluePoint Laboratories NADOLOL 80 mg/1 100 TABLET in 1 BOTTLE (68001-319-00)
76282-347-01 76282-347 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20200727 N/A ANDA ANDA203455 Exelan Pharmaceuticals Inc. NADOLOL 20 mg/1 100 TABLET in 1 BOTTLE (76282-347-01)
76282-348-01 76282-348 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20200727 N/A ANDA ANDA203455 Exelan Pharmaceuticals Inc. NADOLOL 40 mg/1 100 TABLET in 1 BOTTLE (76282-348-01)
76282-349-01 76282-349 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20200727 N/A ANDA ANDA203455 Exelan Pharmaceuticals Inc. NADOLOL 80 mg/1 100 TABLET in 1 BOTTLE (76282-349-01)
0904-7070-07 0904-7070 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Major Pharmaceuticals NADOLOL 20 mg/1 30 BLISTER PACK in 1 CARTON (0904-7070-07) / 1 TABLET in 1 BLISTER PACK
69097-867-02 69097-867 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 20 mg/1 30 TABLET in 1 BOTTLE (69097-867-02)
69097-867-07 69097-867 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 20 mg/1 100 TABLET in 1 BOTTLE (69097-867-07)
69097-867-15 69097-867 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 20 mg/1 1000 TABLET in 1 BOTTLE (69097-867-15)
69097-868-02 69097-868 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 40 mg/1 30 TABLET in 1 BOTTLE (69097-868-02)
69097-868-07 69097-868 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 40 mg/1 100 TABLET in 1 BOTTLE (69097-868-07)
69097-868-15 69097-868 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 40 mg/1 1000 TABLET in 1 BOTTLE (69097-868-15)
69097-869-02 69097-869 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 80 mg/1 30 TABLET in 1 BOTTLE (69097-869-02)
69097-869-07 69097-869 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 80 mg/1 100 TABLET in 1 BOTTLE (69097-869-07)
69097-869-15 69097-869 HUMAN PRESCRIPTION DRUG Nadolol Nadolol TABLET ORAL 20160223 N/A ANDA ANDA203455 Cipla USA Inc. NADOLOL 80 mg/1 1000 TABLET in 1 BOTTLE (69097-869-15)
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