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
51655-446-20 51655-446 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20201002 N/A ANDA ANDA078420 Northwind Pharmaceuticals NABUMETONE 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-446-20)
51655-446-25 51655-446 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220504 N/A ANDA ANDA078420 Northwind Pharmaceuticals NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (51655-446-25)
51655-446-52 51655-446 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20201223 N/A ANDA ANDA078420 Northwind Pharmaceuticals NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-446-52)
51655-446-84 51655-446 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220128 N/A ANDA ANDA078420 Northwind Pharmaceuticals NABUMETONE 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (51655-446-84)
76420-210-07 76420-210 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220308 N/A ANDA ANDA078420 Asclemed USA, Inc. NABUMETONE 500 mg/1 7 TABLET in 1 BOTTLE (76420-210-07)
76420-210-10 76420-210 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220308 N/A ANDA ANDA078420 Asclemed USA, Inc. NABUMETONE 500 mg/1 10 TABLET in 1 BOTTLE (76420-210-10)
71335-1559-3 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 30 TABLET in 1 BOTTLE (71335-1559-3)
71335-1559-4 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 20 TABLET in 1 BOTTLE (71335-1559-4)
71335-1559-5 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 42 TABLET in 1 BOTTLE (71335-1559-5)
71335-1559-6 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 100 TABLET in 1 BOTTLE (71335-1559-6)
71335-1559-7 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 14 TABLET in 1 BOTTLE (71335-1559-7)
71335-1559-8 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 6 TABLET in 1 BOTTLE (71335-1559-8)
71335-1559-9 71335-1559 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220210 N/A ANDA ANDA078420 Bryant Ranch Prepack NABUMETONE 750 mg/1 9 TABLET in 1 BOTTLE (71335-1559-9)
45865-111-60 45865-111 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200701 N/A ANDA ANDA078420 Medsource Pharmaceuticals NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE (45865-111-60)
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)
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)
76420-210-14 76420-210 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220308 N/A ANDA ANDA078420 Asclemed USA, Inc. NABUMETONE 500 mg/1 14 TABLET in 1 BOTTLE (76420-210-14)
76420-210-20 76420-210 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220308 N/A ANDA ANDA078420 Asclemed USA, Inc. NABUMETONE 500 mg/1 20 TABLET in 1 BOTTLE (76420-210-20)
76420-210-30 76420-210 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220308 N/A ANDA ANDA078420 Asclemed USA, Inc. NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE (76420-210-30)
76420-210-60 76420-210 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20220308 N/A ANDA ANDA078420 Asclemed USA, Inc. NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE (76420-210-60)
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