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
0009-0031-01	0009-0031	HUMAN PRESCRIPTION DRUG	CORTEF	hydrocortisone	TABLET	ORAL	19521215	N/A	NDA	NDA008697	Pharmacia & Upjohn Company LLC	HYDROCORTISONE	10 mg/1	100 TABLET in 1 BOTTLE (0009-0031-01)
59762-0075-1	59762-0075	HUMAN PRESCRIPTION DRUG	Hydrocortisone	hydrocortisone	TABLET	ORAL	20130220	N/A	NDA AUTHORIZED GENERIC	NDA008697	Greenstone LLC	HYDROCORTISONE	20 mg/1	100 TABLET in 1 BOTTLE (59762-0075-1)
0009-0012-01	0009-0012	HUMAN PRESCRIPTION DRUG	CORTEF	hydrocortisone	TABLET	ORAL	19521215	N/A	NDA	NDA008697	Pharmacia & Upjohn Company LLC	HYDROCORTISONE	5 mg/1	50 TABLET in 1 BOTTLE (0009-0012-01)
59762-0074-1	59762-0074	HUMAN PRESCRIPTION DRUG	Hydrocortisone	hydrocortisone	TABLET	ORAL	20130220	N/A	NDA AUTHORIZED GENERIC	NDA008697	Greenstone LLC	HYDROCORTISONE	10 mg/1	100 TABLET in 1 BOTTLE (59762-0074-1)
59762-0073-1	59762-0073	HUMAN PRESCRIPTION DRUG	Hydrocortisone	hydrocortisone	TABLET	ORAL	20130220	N/A	NDA AUTHORIZED GENERIC	NDA008697	Greenstone LLC	HYDROCORTISONE	5 mg/1	50 TABLET in 1 BOTTLE (59762-0073-1)
76420-028-50	76420-028	HUMAN PRESCRIPTION DRUG	Hydrocortisone	hydrocortisone	TABLET	ORAL	20191224	N/A	NDA AUTHORIZED GENERIC	NDA008697	Asclemed USA, Inc.	HYDROCORTISONE	5 mg/1	50 TABLET in 1 BOTTLE (76420-028-50)
76420-028-90	76420-028	HUMAN PRESCRIPTION DRUG	Hydrocortisone	hydrocortisone	TABLET	ORAL	20191224	N/A	NDA AUTHORIZED GENERIC	NDA008697	Asclemed USA, Inc.	HYDROCORTISONE	5 mg/1	90 TABLET in 1 BOTTLE (76420-028-90)
0009-0044-01	0009-0044	HUMAN PRESCRIPTION DRUG	CORTEF	hydrocortisone	TABLET	ORAL	19521215	N/A	NDA	NDA008697	Pharmacia & Upjohn Company LLC	HYDROCORTISONE	20 mg/1	100 TABLET in 1 BOTTLE (0009-0044-01)