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）

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
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)
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)
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)
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)
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)
0054-0017-20	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
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)