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
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	N/A	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
68071-2543-6	68071-2543	HUMAN PRESCRIPTION DRUG	azithromycin	azithromycin	TABLET, FILM COATED	ORAL	20210927	N/A	NDA AUTHORIZED GENERIC	NDA050711	NuCare Pharmaceuticals,Inc.	AZITHROMYCIN DIHYDRATE	250 mg/1	6 TABLET, FILM COATED in 1 BLISTER PACK (68071-2543-6)
59762-2198-3	59762-2198	HUMAN PRESCRIPTION DRUG	azithromycin	azithromycin	TABLET, FILM COATED	ORAL	20190513	N/A	NDA AUTHORIZED GENERIC	NDA050711	Greenstone LLC	AZITHROMYCIN DIHYDRATE	250 mg/1	3 BLISTER PACK in 1 CARTON (59762-2198-3) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59762-2198-1)
59762-2198-7	59762-2198	HUMAN PRESCRIPTION DRUG	azithromycin	azithromycin	TABLET, FILM COATED	ORAL	20190513	N/A	NDA AUTHORIZED GENERIC	NDA050711	Greenstone LLC	AZITHROMYCIN DIHYDRATE	250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59762-2198-7)
67296-1870-6	67296-1870	HUMAN PRESCRIPTION DRUG	azithromycin	azithromycin	TABLET, FILM COATED	ORAL	20190513	N/A	NDA AUTHORIZED GENERIC	NDA050711	RedPharm Drug, Inc.	AZITHROMYCIN DIHYDRATE	250 mg/1	6 TABLET, FILM COATED in 1 BOX (67296-1870-6)