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
67296-1444-7	67296-1444	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20200206	N/A	ANDA	ANDA083677	Redpharm Drug, Inc.	PREDNISONE	20 mg/1	15 TABLET in 1 BOTTLE (67296-1444-7)
67296-1444-2	67296-1444	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20200211	N/A	ANDA	ANDA083677	Redpharm Drug, Inc.	PREDNISONE	20 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (67296-1444-2)
67296-1444-1	67296-1444	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20200206	N/A	ANDA	ANDA083677	Redpharm Drug, Inc.	PREDNISONE	20 mg/1	10 TABLET in 1 BOTTLE (67296-1444-1)
0378-0642-01	0378-0642	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20200211	N/A	ANDA	ANDA083677	Mylan Pharmaceuticals Inc.	PREDNISONE	20 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0378-0642-01)
0378-0642-05	0378-0642	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20200206	N/A	ANDA	ANDA083677	Mylan Pharmaceuticals Inc.	PREDNISONE	20 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (0378-0642-05)
0378-0642-10	0378-0642	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20200211	N/A	ANDA	ANDA083677	Mylan Pharmaceuticals Inc.	PREDNISONE	20 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0378-0642-10)
51407-923-05	51407-923	HUMAN PRESCRIPTION DRUG	Prednisone	Prednisone	TABLET	ORAL	20240714	N/A	ANDA	ANDA083677	Golden State Medical Supply, Inc.	PREDNISONE	20 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (51407-923-05)