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=ANDA085162"
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
71205-362-15 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201123 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 15 TABLET in 1 BOTTLE (71205-362-15)
71205-362-18 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20200114 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 18 TABLET in 1 BOTTLE (71205-362-18)
71205-362-20 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201221 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 20 TABLET in 1 BOTTLE (71205-362-20)
71205-362-24 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201221 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 24 TABLET in 1 BOTTLE (71205-362-24)
71205-362-28 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20210225 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 28 TABLET in 1 BOTTLE (71205-362-28)
71205-362-12 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201221 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 12 TABLET in 1 BOTTLE (71205-362-12)
71205-362-10 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20201221 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 10 TABLET in 1 BOTTLE (71205-362-10)
71205-362-06 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20191101 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 6 TABLET in 1 BOTTLE (71205-362-06)
71205-362-63 71205-362 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20230612 N/A ANDA ANDA085162 Proficient Rx LP PREDNISONE 10 mg/1 63 TABLET in 1 BOTTLE (71205-362-63)
0591-5442-21 0591-5442 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20160525 N/A ANDA ANDA085162 Actavis Pharma, Inc. PREDNISONE 10 mg/1 1 BLISTER PACK in 1 CARTON (0591-5442-21) / 21 TABLET in 1 BLISTER PACK
0591-5442-01 0591-5442 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19900101 N/A ANDA ANDA085162 Actavis Pharma, Inc. PREDNISONE 10 mg/1 100 TABLET in 1 BOTTLE (0591-5442-01)
67296-0140-1 67296-0140 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20200422 N/A ANDA ANDA085162 RedPharm Drug Inc. PREDNISONE 10 mg/1 10 TABLET in 1 BOTTLE (67296-0140-1)
67296-0140-2 67296-0140 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20110624 N/A ANDA ANDA085162 RedPharm Drug Inc. PREDNISONE 10 mg/1 30 TABLET in 1 BOTTLE (67296-0140-2)
67296-0140-3 67296-0140 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20200422 N/A ANDA ANDA085162 RedPharm Drug Inc. PREDNISONE 10 mg/1 42 TABLET in 1 BOTTLE (67296-0140-3)
67296-0140-9 67296-0140 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20200422 N/A ANDA ANDA085162 RedPharm Drug Inc. PREDNISONE 10 mg/1 9 TABLET in 1 BOTTLE (67296-0140-9)
0591-5442-05 0591-5442 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19900101 N/A ANDA ANDA085162 Actavis Pharma, Inc. PREDNISONE 10 mg/1 500 TABLET in 1 BOTTLE (0591-5442-05)
0591-5442-10 0591-5442 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 19930518 N/A ANDA ANDA085162 Actavis Pharma, Inc. PREDNISONE 10 mg/1 1000 TABLET in 1 BOTTLE (0591-5442-10)
0591-5442-43 0591-5442 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20160525 N/A ANDA ANDA085162 Actavis Pharma, Inc. PREDNISONE 10 mg/1 1 BLISTER PACK in 1 CARTON (0591-5442-43) / 48 TABLET in 1 BLISTER PACK
51655-410-49 51655-410 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20140428 N/A ANDA ANDA085162 Northwind Pharmaceuticals, LLC PREDNISONE 10 mg/1 42 TABLET in 1 BOTTLE (51655-410-49)
51655-410-52 51655-410 HUMAN PRESCRIPTION DRUG Prednisone Prednisone TABLET ORAL 20200410 N/A ANDA ANDA085162 Northwind Pharmaceuticals, LLC PREDNISONE 10 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-410-52)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase