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=ANDA084122"
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
51655-493-49 51655-493 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20210113 N/A ANDA ANDA084122 Northwind Pharmaceuticals PREDNISONE 10 mg/1 42 TABLET in 1 BOTTLE, PLASTIC (51655-493-49)
70518-4191-0 70518-4191 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20240930 N/A ANDA ANDA084122 REMEDYREPACK INC. PREDNISONE 10 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-4191-0)
70518-4191-1 70518-4191 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20240930 N/A ANDA ANDA084122 REMEDYREPACK INC. PREDNISONE 10 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-4191-1)
70518-4191-2 70518-4191 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20240930 N/A ANDA ANDA084122 REMEDYREPACK INC. PREDNISONE 10 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (70518-4191-2)
70518-4191-3 70518-4191 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20241106 N/A ANDA ANDA084122 REMEDYREPACK INC. PREDNISONE 10 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-4191-3)
51655-726-21 51655-726 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20210610 N/A ANDA ANDA084122 Northwind Pharmaceuticals, LLC PREDNISONE 10 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (51655-726-21)
0054-9817-25 0054-9817 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200323 N/A ANDA ANDA084122 Hikma Pharmaceuticals USA Inc. PREDNISONE 10 mg/1 100 TABLET in 1 BOTTLE (0054-9817-25)
0054-9817-29 0054-9817 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200323 N/A ANDA ANDA084122 Hikma Pharmaceuticals USA Inc. PREDNISONE 10 mg/1 500 TABLET in 1 BOTTLE (0054-9817-29)
51407-358-05 51407-358 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20200226 N/A ANDA ANDA084122 Golden State Medical Supply, Inc. PREDNISONE 10 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (51407-358-05)
42708-045-21 42708-045 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20180317 N/A ANDA ANDA084122 QPharma, Inc. PREDNISONE 10 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (42708-045-21)
0054-0017-20 0054-0017 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20030213 N/A ANDA ANDA084122 Hikma Pharmaceuticals USA Inc. PREDNISONE 10 mg/1 10 BLISTER PACK in 1 CARTON (0054-0017-20) / 10 TABLET in 1 BLISTER PACK
0054-0017-25 0054-0017 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20030213 N/A ANDA ANDA084122 Hikma Pharmaceuticals USA Inc. PREDNISONE 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0054-0017-25)
0054-0017-29 0054-0017 HUMAN PRESCRIPTION DRUG PredniSONE PredniSONE TABLET ORAL 20030213 N/A ANDA ANDA084122 Hikma Pharmaceuticals USA Inc. PREDNISONE 10 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (0054-0017-29)
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