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
70518-4191-4	70518-4191	HUMAN PRESCRIPTION DRUG	PredniSONE	PredniSONE	TABLET	ORAL	20250414	N/A	ANDA	ANDA084122	REMEDYREPACK INC.	PREDNISONE	10 mg/1	18 TABLET in 1 BOTTLE, PLASTIC (70518-4191-4)
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)
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)
80425-0485-1	80425-0485	HUMAN PRESCRIPTION DRUG	PredniSONE	PredniSONE	TABLET	ORAL	20250214	N/A	ANDA	ANDA084122	Advanced Rx of Tennessee, LLC	PREDNISONE	10 mg/1	21 TABLET in 1 BOTTLE (80425-0485-1)
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 Health Company, LLC	PREDNISONE	10 mg/1	42 TABLET in 1 BOTTLE, PLASTIC (51655-493-49)