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
42708-115-21	42708-115	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20180420	N/A	ANDA	ANDA085162	QPharma, Inc.	PREDNISONE	10 mg/1	21 TABLET in 1 BOTTLE (42708-115-21)
80425-0491-1	80425-0491	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20250317	N/A	ANDA	ANDA085162	Advanced Rx of Tennessee, LLC	PREDNISONE	10 mg/1	1 BLISTER PACK in 1 CARTON (80425-0491-1) / 21 TABLET in 1 BLISTER PACK
51655-410-20	51655-410	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20140428	N/A	ANDA	ANDA085162	Northwind Pharmaceuticals, LLC	PREDNISONE	10 mg/1	20 TABLET in 1 BOTTLE (51655-410-20)
51655-410-21	51655-410	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20210610	N/A	ANDA	ANDA085162	Northwind Pharmaceuticals, LLC	PREDNISONE	10 mg/1	21 TABLET in 1 BOTTLE, PLASTIC (51655-410-21)
51655-410-27	51655-410	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20230303	N/A	ANDA	ANDA085162	Northwind Pharmaceuticals, LLC	PREDNISONE	10 mg/1	12 TABLET in 1 BOTTLE, PLASTIC (51655-410-27)
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)
51655-410-53	51655-410	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20230315	N/A	ANDA	ANDA085162	Northwind Pharmaceuticals, LLC	PREDNISONE	10 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (51655-410-53)
51655-410-54	51655-410	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20210512	N/A	ANDA	ANDA085162	Northwind Pharmaceuticals, LLC	PREDNISONE	10 mg/1	15 TABLET in 1 BOTTLE, PLASTIC (51655-410-54)
72189-646-21	72189-646	HUMAN PRESCRIPTION DRUG	Prednisone D/P	Prednisone D/P	TABLET	ORAL	20251021	N/A	ANDA	ANDA085162	Direct_Rx	PREDNISONE	10 mg/1	21 TABLET in 1 CARTON (72189-646-21)
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)
0591-5442-01	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)
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)
0591-5442-21	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
0591-5442-43	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
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)