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
81665-103-10	81665-103	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	20240502	N/A	NDA AUTHORIZED GENERIC	NDA020215	OMNIVIUM PHARMACEUTICALS LLC.	ISOSORBIDE MONONITRATE	20 mg/1	100 TABLET in 1 BOTTLE (81665-103-10)
81665-102-10	81665-102	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	20240502	N/A	NDA AUTHORIZED GENERIC	NDA020215	OMNIVIUM PHARMACEUTICALS LLC.	ISOSORBIDE MONONITRATE	10 mg/1	100 TABLET in 1 BOTTLE (81665-102-10)
63187-900-60	63187-900	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	20170901	N/A	NDA AUTHORIZED GENERIC	NDA020215	Proficient Rx LP	ISOSORBIDE MONONITRATE	20 mg/1	60 TABLET in 1 BOTTLE (63187-900-60)
63187-900-90	63187-900	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	20170901	N/A	NDA AUTHORIZED GENERIC	NDA020215	Proficient Rx LP	ISOSORBIDE MONONITRATE	20 mg/1	90 TABLET in 1 BOTTLE (63187-900-90)
62175-107-01	62175-107	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	19930630	N/A	NDA AUTHORIZED GENERIC	NDA020215	Lannett Company, Inc.	ISOSORBIDE MONONITRATE	20 mg/1	100 TABLET in 1 BOTTLE (62175-107-01)
62175-106-01	62175-106	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	19930630	N/A	NDA AUTHORIZED GENERIC	NDA020215	Lannett Company, Inc.	ISOSORBIDE MONONITRATE	10 mg/1	100 TABLET in 1 BOTTLE (62175-106-01)
63187-900-30	63187-900	HUMAN PRESCRIPTION DRUG	isosorbide mononitrate	isosorbide mononitrate	TABLET	ORAL	20170901	N/A	NDA AUTHORIZED GENERIC	NDA020215	Proficient Rx LP	ISOSORBIDE MONONITRATE	20 mg/1	30 TABLET in 1 BOTTLE (63187-900-30)