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
71335-1391-1 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191209 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 20 TABLET in 1 BOTTLE (71335-1391-1)
71335-1391-2 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191220 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE (71335-1391-2)
71335-1391-3 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191114 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE (71335-1391-3)
71335-1391-4 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191107 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 90 TABLET in 1 BOTTLE (71335-1391-4)
71335-1391-5 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20211228 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 42 TABLET in 1 BOTTLE (71335-1391-5)
71335-1391-6 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200713 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 56 TABLET in 1 BOTTLE (71335-1391-6)
71335-1391-7 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20211228 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 14 TABLET in 1 BOTTLE (71335-1391-7)
71335-1391-8 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20211228 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 100 TABLET in 1 BOTTLE (71335-1391-8)
71335-1391-9 71335-1391 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20211228 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 500 mg/1 9 TABLET in 1 BOTTLE (71335-1391-9)
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)
55700-845-30 55700-845 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200228 N/A ANDA ANDA078420 Quality Care Products, LLC NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE (55700-845-30)
55700-845-60 55700-845 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200228 N/A ANDA ANDA078420 Quality Care Products, LLC NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE (55700-845-60)
71205-530-30 71205-530 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210203 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 30 TABLET in 1 BOTTLE (71205-530-30)
71205-530-60 71205-530 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210203 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE (71205-530-60)
71205-530-90 71205-530 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210203 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 90 TABLET in 1 BOTTLE (71205-530-90)
72789-040-30 72789-040 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191217 N/A ANDA ANDA078420 PD-Rx Pharmaceuticals, Inc. NABUMETONE 750 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-040-30)
50090-5294-0 50090-5294 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20201023 N/A ANDA ANDA078420 A-S Medication Solutions NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE (50090-5294-0)
50090-5294-7 50090-5294 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20201023 N/A ANDA ANDA078420 A-S Medication Solutions NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE (50090-5294-7)
50090-5294-8 50090-5294 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20201023 N/A ANDA ANDA078420 A-S Medication Solutions NABUMETONE 500 mg/1 90 TABLET in 1 BOTTLE (50090-5294-8)
60760-369-14 60760-369 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191010 N/A ANDA ANDA078420 St. Mary's Medical Park Pharmacy NABUMETONE 750 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (60760-369-14)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase