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
51655-765-21	51655-765	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20210730	N/A	ANDA	ANDA080292	Northwind Pharmaceuticals	PREDNISONE	5 mg/1	21 TABLET in 1 BOTTLE, PLASTIC (51655-765-21)
51407-921-10	51407-921	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20240714	N/A	ANDA	ANDA080292	Golden State Medical Supply, Inc.	PREDNISONE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (51407-921-10)
72162-2149-0	72162-2149	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190307	N/A	ANDA	ANDA080292	Bryant Ranch Prepack	PREDNISONE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72162-2149-0)
0378-0640-01	0378-0640	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190307	N/A	ANDA	ANDA080292	Mylan Pharmaceuticals Inc.	PREDNISONE	5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0378-0640-01)
0378-0640-10	0378-0640	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190307	N/A	ANDA	ANDA080292	Mylan Pharmaceuticals Inc.	PREDNISONE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0378-0640-10)
42708-136-21	42708-136	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20210423	N/A	ANDA	ANDA080292	QPharma Inc	PREDNISONE	5 mg/1	21 TABLET in 1 BOTTLE, PLASTIC (42708-136-21)
67296-1331-7	67296-1331	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20210101	N/A	ANDA	ANDA080292	RedPharm Drug, Inc.	PREDNISONE	5 mg/1	21 TABLET in 1 BOTTLE (67296-1331-7)