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=ANDA080292"
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
51655-765-21 51655-765 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20210730 N/A ANDA ANDA080292 Northwind Pharmaceuticals PREDNISONE 5 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (51655-765-21)
51407-921-10 51407-921 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20240714 N/A ANDA ANDA080292 Golden State Medical Supply, Inc. PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (51407-921-10)
72162-2149-0 72162-2149 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190307 N/A ANDA ANDA080292 Bryant Ranch Prepack PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (72162-2149-0)
0378-0640-01 0378-0640 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190307 N/A ANDA ANDA080292 Mylan Pharmaceuticals Inc. PREDNISONE 5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0378-0640-01)
0378-0640-10 0378-0640 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190307 N/A ANDA ANDA080292 Mylan Pharmaceuticals Inc. PREDNISONE 5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0640-10)
42708-136-21 42708-136 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20210423 N/A ANDA ANDA080292 QPharma Inc PREDNISONE 5 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (42708-136-21)
67296-1331-7 67296-1331 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20210101 N/A ANDA ANDA080292 RedPharm Drug, Inc. PREDNISONE 5 mg/1 21 TABLET in 1 BOTTLE (67296-1331-7)
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