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=ANDA085161"
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
50090-2786-0 50090-2786 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20170117 N/A ANDA ANDA085161 A-S Medication Solutions PREDNISONE 20 mg/1 21 TABLET in 1 BOTTLE (50090-2786-0)
0591-5443-01 0591-5443 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19900101 N/A ANDA ANDA085161 Actavis Pharma, Inc. PREDNISONE 20 mg/1 100 TABLET in 1 BOTTLE (0591-5443-01)
0591-5443-05 0591-5443 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19900101 N/A ANDA ANDA085161 Actavis Pharma, Inc. PREDNISONE 20 mg/1 500 TABLET in 1 BOTTLE (0591-5443-05)
0591-5443-10 0591-5443 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19931111 N/A ANDA ANDA085161 Actavis Pharma, Inc. PREDNISONE 20 mg/1 1000 TABLET in 1 BOTTLE (0591-5443-10)
67296-0138-1 67296-0138 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190101 N/A ANDA ANDA085161 RedPharm Drug, Inc. PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (67296-0138-1)
67296-0138-2 67296-0138 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190101 N/A ANDA ANDA085161 RedPharm Drug, Inc. PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE (67296-0138-2)
67296-0138-3 67296-0138 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19900101 N/A ANDA ANDA085161 RedPharm Drug, Inc. PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (67296-0138-3)
67296-0138-4 67296-0138 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19900101 N/A ANDA ANDA085161 RedPharm Drug, Inc. PREDNISONE 20 mg/1 30 TABLET in 1 BOTTLE (67296-0138-4)
51655-242-53 51655-242 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230306 N/A ANDA ANDA085161 Northwind Pharmaceuticals, LLC PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (51655-242-53)
68071-4685-2 68071-4685 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20181231 N/A ANDA ANDA085161 NuCare Pharmaceuticals,Inc. PREDNISONE 20 mg/1 21 TABLET in 1 BOTTLE (68071-4685-2)
42708-105-10 42708-105 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20180418 N/A ANDA ANDA085161 QPharma, Inc. PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (42708-105-10)
71205-239-05 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 5 TABLET in 1 BOTTLE (71205-239-05)
71205-239-06 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 6 TABLET in 1 BOTTLE (71205-239-06)
71205-239-07 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 7 TABLET in 1 BOTTLE (71205-239-07)
71205-239-10 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 10 TABLET in 1 BOTTLE (71205-239-10)
71205-239-12 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 12 TABLET in 1 BOTTLE (71205-239-12)
71205-239-14 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 14 TABLET in 1 BOTTLE (71205-239-14)
71205-239-15 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 15 TABLET in 1 BOTTLE (71205-239-15)
71205-239-18 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 18 TABLET in 1 BOTTLE (71205-239-18)
71205-239-20 71205-239 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20190301 N/A ANDA ANDA085161 Proficient Rx LP PREDNISONE 20 mg/1 20 TABLET in 1 BOTTLE (71205-239-20)
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