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=ANDA078420"
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
68788-7597-8 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 120 TABLET in 1 BOTTLE (68788-7597-8)
68788-7597-9 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 90 TABLET in 1 BOTTLE (68788-7597-9)
70518-4047-0 70518-4047 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20240407 N/A ANDA ANDA078420 REMEDYREPACK INC. NABUMETONE 750 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-4047-0)
70518-4047-1 70518-4047 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20240516 N/A ANDA ANDA078420 REMEDYREPACK INC. NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-4047-1)
71335-2292-1 71335-2292 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20231201 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 500 TABLET in 1 BOTTLE (71335-2292-1)
71335-2293-1 71335-2293 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20231201 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 500 TABLET in 1 BOTTLE (71335-2293-1)
71205-977-00 71205-977 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 500 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71205-977-00)
71205-977-30 71205-977 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71205-977-30)
71205-977-55 71205-977 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 500 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (71205-977-55)
71205-977-60 71205-977 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71205-977-60)
71205-977-72 71205-977 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 500 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (71205-977-72)
71205-977-90 71205-977 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 500 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71205-977-90)
71205-978-00 71205-978 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71205-978-00)
71205-978-30 71205-978 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71205-978-30)
71205-978-55 71205-978 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55)
71205-978-60 71205-978 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71205-978-60)
71205-978-72 71205-978 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (71205-978-72)
71205-978-90 71205-978 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200507 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71205-978-90)
68788-7765-1 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 100 TABLET in 1 BOTTLE (68788-7765-1)
68788-7765-2 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 20 TABLET in 1 BOTTLE (68788-7765-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase