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
68071-3958-9	68071-3958	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20260126	N/A	ANDA	ANDA215671	NuCare Pharmaceuticals, Inc.	PREDNISONE	1 mg/1	90 TABLET in 1 BOTTLE (68071-3958-9)
71335-2273-2	71335-2273	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20231205	N/A	ANDA	ANDA215671	Bryant Ranch Prepack	PREDNISONE	1 mg/1	30 TABLET in 1 BOTTLE (71335-2273-2)
71335-2273-1	71335-2273	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20231102	N/A	ANDA	ANDA215671	Bryant Ranch Prepack	PREDNISONE	1 mg/1	100 TABLET in 1 BOTTLE (71335-2273-1)
59651-484-78	59651-484	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20211116	N/A	ANDA	ANDA215671	Aurobindo Pharma Limited	PREDNISONE	1 mg/1	10 BLISTER PACK in 1 CARTON (59651-484-78) / 10 TABLET in 1 BLISTER PACK
59651-484-01	59651-484	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20211116	N/A	ANDA	ANDA215671	Aurobindo Pharma Limited	PREDNISONE	1 mg/1	100 TABLET in 1 BOTTLE (59651-484-01)
59651-484-99	59651-484	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20211116	N/A	ANDA	ANDA215671	Aurobindo Pharma Limited	PREDNISONE	1 mg/1	1000 TABLET in 1 BOTTLE (59651-484-99)