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=ANDA078314"
符合检索条件的记录共 17 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
68462-178-01 68462-178 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20070801 N/A ANDA ANDA078314 Glenmark Pharmaceuticals Inc., USA NAPROXEN SODIUM 275 mg/1 100 TABLET in 1 BOTTLE (68462-178-01)
68462-178-05 68462-178 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20070801 N/A ANDA ANDA078314 Glenmark Pharmaceuticals Inc., USA NAPROXEN SODIUM 275 mg/1 500 TABLET in 1 BOTTLE (68462-178-05)
71335-3075-0 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 6 TABLET in 1 BOTTLE (71335-3075-0)
71335-3075-1 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 20 TABLET in 1 BOTTLE (71335-3075-1)
71335-3075-2 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 100 TABLET in 1 BOTTLE (71335-3075-2)
71335-3075-3 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 30 TABLET in 1 BOTTLE (71335-3075-3)
71335-3075-4 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 120 TABLET in 1 BOTTLE (71335-3075-4)
71335-3075-5 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 60 TABLET in 1 BOTTLE (71335-3075-5)
71335-3075-6 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 90 TABLET in 1 BOTTLE (71335-3075-6)
71335-3075-7 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 42 TABLET in 1 BOTTLE (71335-3075-7)
71335-3075-8 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 14 TABLET in 1 BOTTLE (71335-3075-8)
71335-3075-9 71335-3075 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20260209 N/A ANDA ANDA078314 Bryant Ranch Prepack NAPROXEN SODIUM 550 mg/1 56 TABLET in 1 BOTTLE (71335-3075-9)
80425-0532-1 80425-0532 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20250602 N/A ANDA ANDA078314 Advanced Rx of Tennessee, LLC NAPROXEN SODIUM 550 mg/1 30 TABLET in 1 BOTTLE (80425-0532-1)
80425-0532-2 80425-0532 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20250602 N/A ANDA ANDA078314 Advanced Rx of Tennessee, LLC NAPROXEN SODIUM 550 mg/1 60 TABLET in 1 BOTTLE (80425-0532-2)
80425-0532-3 80425-0532 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20250602 N/A ANDA ANDA078314 Advanced Rx of Tennessee, LLC NAPROXEN SODIUM 550 mg/1 90 TABLET in 1 BOTTLE (80425-0532-3)
68462-179-01 68462-179 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20070801 N/A ANDA ANDA078314 Glenmark Pharmaceuticals Inc., USA NAPROXEN SODIUM 550 mg/1 100 TABLET in 1 BOTTLE (68462-179-01)
68462-179-05 68462-179 HUMAN PRESCRIPTION DRUG Naproxen Sodium Naproxen Sodium TABLET ORAL 20070801 N/A ANDA ANDA078314 Glenmark Pharmaceuticals Inc., USA NAPROXEN SODIUM 550 mg/1 500 TABLET in 1 BOTTLE (68462-179-05)
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