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
67296-0020-1	67296-0020	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	19960718	N/A	NDA	NDA050711	Redpharm Drug	AZITHROMYCIN DIHYDRATE	250 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (67296-0020-1)
67296-0020-2	67296-0020	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	19960718	N/A	NDA	NDA050711	Redpharm Drug	AZITHROMYCIN DIHYDRATE	250 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (67296-0020-2)
0069-3060-75	0069-3060	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	19960718	N/A	NDA	NDA050711	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	250 mg/1	3 BLISTER PACK in 1 BOX (0069-3060-75) / 6 TABLET, FILM COATED in 1 BLISTER PACK
0069-4061-01	0069-4061	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	20200504	N/A	NDA	NDA050711	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-4061-01)
0069-4061-89	0069-4061	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	20190718	20260430	NDA	NDA050711	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	250 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (0069-4061-89) / 1 TABLET, FILM COATED in 1 BLISTER PACK