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
0024-5852-30	0024-5852	HUMAN PRESCRIPTION DRUG	Avapro	irbesartan	TABLET, FILM COATED	ORAL	20130101	N/A	NDA	NDA020757	Sanofi-Aventis U.S. LLC	IRBESARTAN	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0024-5852-30)
0024-5851-30	0024-5851	HUMAN PRESCRIPTION DRUG	Avapro	irbesartan	TABLET, FILM COATED	ORAL	20130101	N/A	NDA	NDA020757	Sanofi-Aventis U.S. LLC	IRBESARTAN	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0024-5851-30)
0024-5850-90	0024-5850	HUMAN PRESCRIPTION DRUG	Avapro	irbesartan	TABLET, FILM COATED	ORAL	20130101	20250531	NDA	NDA020757	Sanofi-Aventis U.S. LLC	IRBESARTAN	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0024-5850-90)
71205-404-30	71205-404	HUMAN PRESCRIPTION DRUG	Irbesartan	irbesartan	TABLET, FILM COATED	ORAL	20200217	N/A	NDA AUTHORIZED GENERIC	NDA020757	Proficient Rx LP	IRBESARTAN	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-404-30)
71205-404-60	71205-404	HUMAN PRESCRIPTION DRUG	Irbesartan	irbesartan	TABLET, FILM COATED	ORAL	20200217	N/A	NDA AUTHORIZED GENERIC	NDA020757	Proficient Rx LP	IRBESARTAN	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-404-60)
71205-404-90	71205-404	HUMAN PRESCRIPTION DRUG	Irbesartan	irbesartan	TABLET, FILM COATED	ORAL	20200217	N/A	NDA AUTHORIZED GENERIC	NDA020757	Proficient Rx LP	IRBESARTAN	75 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-404-90)