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
68071-4691-1	68071-4691	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190103	N/A	ANDA	ANDA085161	NuCare Pharmaceuticals,Inc.	PREDNISONE	20 mg/1	10 TABLET in 1 BOTTLE (68071-4691-1)
68071-4691-4	68071-4691	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190103	N/A	ANDA	ANDA085161	NuCare Pharmaceuticals,Inc.	PREDNISONE	20 mg/1	4 TABLET in 1 BOTTLE (68071-4691-4)
68071-4691-6	68071-4691	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190103	N/A	ANDA	ANDA085161	NuCare Pharmaceuticals,Inc.	PREDNISONE	20 mg/1	6 TABLET in 1 BOTTLE (68071-4691-6)
51655-242-53	51655-242	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20230306	N/A	ANDA	ANDA085161	Northwind Pharmaceuticals, LLC	PREDNISONE	20 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (51655-242-53)
63739-588-10	63739-588	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20140630	N/A	ANDA	ANDA085161	McKesson Corporation dba SKY Packaging	PREDNISONE	20 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-588-10) / 10 TABLET in 1 BLISTER PACK
70518-1561-0	70518-1561	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20181019	N/A	ANDA	ANDA085161	REMEDYREPACK INC.	PREDNISONE	20 mg/1	30 TABLET in 1 BLISTER PACK (70518-1561-0)
70518-1561-1	70518-1561	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20191023	N/A	ANDA	ANDA085161	REMEDYREPACK INC.	PREDNISONE	20 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (70518-1561-1)
53002-3252-1	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	5 TABLET in 1 BOTTLE (53002-3252-1)
53002-3252-2	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	6 TABLET in 1 BOTTLE (53002-3252-2)
53002-3252-3	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	9 TABLET in 1 BOTTLE (53002-3252-3)
53002-3252-4	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	12 TABLET in 1 BOTTLE (53002-3252-4)
53002-3252-5	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	13 TABLET in 1 BOTTLE (53002-3252-5)
53002-3252-6	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	14 TABLET in 1 BOTTLE (53002-3252-6)
53002-3252-7	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	19 TABLET in 1 BOTTLE (53002-3252-7)
53002-3252-8	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	17 TABLET in 1 BOTTLE (53002-3252-8)
53002-3252-9	53002-3252	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20190101	N/A	ANDA	ANDA085161	RPK Pharmaceuticals, Inc.	PREDNISONE	20 mg/1	26 TABLET in 1 BOTTLE (53002-3252-9)
42708-105-10	42708-105	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20180418	N/A	ANDA	ANDA085161	QPharma Inc	PREDNISONE	20 mg/1	10 TABLET in 1 BOTTLE (42708-105-10)
70518-2314-3	70518-2314	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20220509	N/A	ANDA	ANDA085161	REMEDYREPACK INC.	PREDNISONE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-2314-3)
0591-5443-01	0591-5443	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	19900101	N/A	ANDA	ANDA085161	Actavis Pharma, Inc.	PREDNISONE	20 mg/1	100 TABLET in 1 BOTTLE (0591-5443-01)
0591-5443-05	0591-5443	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	19900101	N/A	ANDA	ANDA085161	Actavis Pharma, Inc.	PREDNISONE	20 mg/1	500 TABLET in 1 BOTTLE (0591-5443-05)