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
59651-488-01	59651-488	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20220328	N/A	ANDA	ANDA215672	Aurobindo Pharma Limited	PREDNISONE	20 mg/1	100 TABLET in 1 BOTTLE (59651-488-01)
59651-488-05	59651-488	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20220328	N/A	ANDA	ANDA215672	Aurobindo Pharma Limited	PREDNISONE	20 mg/1	500 TABLET in 1 BOTTLE (59651-488-05)
59651-488-78	59651-488	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20220328	N/A	ANDA	ANDA215672	Aurobindo Pharma Limited	PREDNISONE	20 mg/1	10 BLISTER PACK in 1 CARTON (59651-488-78) / 10 TABLET in 1 BLISTER PACK
59651-489-01	59651-489	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20220328	N/A	ANDA	ANDA215672	Aurobindo Pharma Limited	PREDNISONE	50 mg/1	100 TABLET in 1 BOTTLE (59651-489-01)
59651-489-78	59651-489	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20220328	N/A	ANDA	ANDA215672	Aurobindo Pharma Limited	PREDNISONE	50 mg/1	10 BLISTER PACK in 1 CARTON (59651-489-78) / 10 TABLET in 1 BLISTER PACK
60760-840-12	60760-840	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20251105	N/A	ANDA	ANDA215672	ST. MARY'S MEDICAL PARK PHARMACY	PREDNISONE	20 mg/1	12 TABLET in 1 BOTTLE, PLASTIC (60760-840-12)
60760-840-21	60760-840	HUMAN PRESCRIPTION DRUG	PREDNISONE	PREDNISONE	TABLET	ORAL	20251229	N/A	ANDA	ANDA215672	ST. MARY'S MEDICAL PARK PHARMACY	PREDNISONE	20 mg/1	21 TABLET in 1 BOTTLE, PLASTIC (60760-840-21)