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
63561-0120-1	63561-0120	HUMAN PRESCRIPTION DRUG	PredniSONE Tablets, USP, 5 mg	PredniSONE	TABLET	ORAL	20240306	N/A	ANDA	ANDA212629	Granulation Technology, Inc.	PREDNISONE	5 mg/1	100 TABLET in 1 BOTTLE (63561-0120-1)
63561-0120-2	63561-0120	HUMAN PRESCRIPTION DRUG	PredniSONE Tablets, USP, 5 mg	PredniSONE	TABLET	ORAL	20240306	N/A	ANDA	ANDA212629	Granulation Technology, Inc.	PREDNISONE	5 mg/1	1000 TABLET in 1 BOTTLE (63561-0120-2)
63561-0121-1	63561-0121	HUMAN PRESCRIPTION DRUG	PredniSONE Tablets, USP, 10 mg	PredniSONE	TABLET	ORAL	20240306	N/A	ANDA	ANDA212629	Granulation Technology, Inc.	PREDNISONE	10 mg/1	100 TABLET in 1 BOTTLE (63561-0121-1)
63561-0121-2	63561-0121	HUMAN PRESCRIPTION DRUG	PredniSONE Tablets, USP, 10 mg	PredniSONE	TABLET	ORAL	20240306	N/A	ANDA	ANDA212629	Granulation Technology, Inc.	PREDNISONE	10 mg/1	1000 TABLET in 1 BOTTLE (63561-0121-2)
63561-0122-1	63561-0122	HUMAN PRESCRIPTION DRUG	PredniSONE Tablets, USP, 20 mg	PredniSONE	TABLET	ORAL	20240306	N/A	ANDA	ANDA212629	Granulation Technology, Inc.	PREDNISONE	20 mg/1	100 TABLET in 1 BOTTLE (63561-0122-1)
63561-0122-2	63561-0122	HUMAN PRESCRIPTION DRUG	PredniSONE Tablets, USP, 20 mg	PredniSONE	TABLET	ORAL	20240306	N/A	ANDA	ANDA212629	Granulation Technology, Inc.	PREDNISONE	20 mg/1	1000 TABLET in 1 BOTTLE (63561-0122-2)