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
0527-2395-19	0527-2395	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20190704	N/A	ANDA	ANDA209044	Lannett Company, Inc.	AZITHROMYCIN DIHYDRATE	500 mg/1	1 BLISTER PACK in 1 CARTON (0527-2395-19) / 3 TABLET, FILM COATED in 1 BLISTER PACK
0527-2395-32	0527-2395	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20190704	N/A	ANDA	ANDA209044	Lannett Company, Inc.	AZITHROMYCIN DIHYDRATE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0527-2395-32)
64980-726-13	64980-726	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209044	Rising Pharma Holdings, Inc.	AZITHROMYCIN DIHYDRATE	500 mg/1	1 BLISTER PACK in 1 CARTON (64980-726-13) / 3 TABLET, FILM COATED in 1 BLISTER PACK
64980-726-03	64980-726	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209044	Rising Pharma Holdings, Inc.	AZITHROMYCIN DIHYDRATE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (64980-726-03)