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=ANDA211575"
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
71335-2160-5 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240528 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 120 TABLET in 1 BOTTLE (71335-2160-5)
71335-2160-6 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240528 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 7 TABLET in 1 BOTTLE (71335-2160-6)
71335-2160-7 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240528 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 20 TABLET in 1 BOTTLE (71335-2160-7)
71335-2160-8 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240528 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 10 TABLET in 1 BOTTLE (71335-2160-8)
71610-834-30 71610-834 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240513 N/A ANDA ANDA211575 Aphena Pharma Solutions - Tennessee, LLC PREDNISONE 5 mg/1 30 TABLET in 1 BOTTLE (71610-834-30)
71610-834-53 71610-834 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240513 N/A ANDA ANDA211575 Aphena Pharma Solutions - Tennessee, LLC PREDNISONE 5 mg/1 60 TABLET in 1 BOTTLE (71610-834-53)
71610-834-60 71610-834 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240513 N/A ANDA ANDA211575 Aphena Pharma Solutions - Tennessee, LLC PREDNISONE 5 mg/1 90 TABLET in 1 BOTTLE (71610-834-60)
71610-834-80 71610-834 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240718 N/A ANDA ANDA211575 Aphena Pharma Solutions - Tennessee, LLC PREDNISONE 5 mg/1 180 TABLET in 1 BOTTLE (71610-834-80)
10135-775-01 10135-775 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 2.5 mg/1 100 TABLET in 1 BOTTLE (10135-775-01)
10135-776-01 10135-776 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 5 mg/1 100 TABLET in 1 BOTTLE (10135-776-01)
10135-776-10 10135-776 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE (10135-776-10)
10135-777-01 10135-777 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 10 mg/1 100 TABLET in 1 BOTTLE (10135-777-01)
10135-777-10 10135-777 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 10 mg/1 1000 TABLET in 1 BOTTLE (10135-777-10)
10135-778-01 10135-778 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 20 mg/1 100 TABLET in 1 BOTTLE (10135-778-01)
10135-778-05 10135-778 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 20 mg/1 500 TABLET in 1 BOTTLE (10135-778-05)
10135-778-10 10135-778 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 20 mg/1 1000 TABLET in 1 BOTTLE (10135-778-10)
10135-779-01 10135-779 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230201 N/A ANDA ANDA211575 Marlex Pharmaceuticals, Inc. PREDNISONE 50 mg/1 100 TABLET in 1 BOTTLE (10135-779-01)
71335-2160-2 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20220927 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 5 TABLET in 1 BOTTLE (71335-2160-2)
71335-2160-3 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240528 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 30 TABLET in 1 BOTTLE (71335-2160-3)
71335-2160-4 71335-2160 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240528 N/A ANDA ANDA211575 Bryant Ranch Prepack PREDNISONE 50 mg/1 60 TABLET in 1 BOTTLE (71335-2160-4)
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