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
70518-0336-0	70518-0336	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	20170320	N/A	NDA	NDA050784	REMEDYREPACK INC.	AZITHROMYCIN DIHYDRATE	500 mg/1	2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0336-0)
70518-0336-2	70518-0336	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	20240305	N/A	NDA	NDA050784	REMEDYREPACK INC.	AZITHROMYCIN DIHYDRATE	500 mg/1	2 POUCH in 1 BOX (70518-0336-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-0336-3)
0069-3070-75	0069-3070	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	20020524	N/A	NDA	NDA050784	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	500 mg/1	3 BLISTER PACK in 1 CARTON (0069-3070-75) / 3 TABLET, FILM COATED in 1 BLISTER PACK
0069-3070-30	0069-3070	HUMAN PRESCRIPTION DRUG	Zithromax	azithromycin dihydrate	TABLET, FILM COATED	ORAL	20020524	N/A	NDA	NDA050784	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-3070-30)