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
53002-2225-1	53002-2225	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	POWDER, FOR SUSPENSION	ORAL	20181001	N/A	NDA AUTHORIZED GENERIC	NDA050693	RPK Pharmaceuticals, Inc.	AZITHROMYCIN DIHYDRATE	1 g/1	3 PACKET in 1 BOX (53002-2225-1) / 1 POWDER, FOR SUSPENSION in 1 PACKET
0069-3051-07	0069-3051	HUMAN PRESCRIPTION DRUG	ZITHROMAX	AZITHROMYCIN DIHYDRATE	POWDER, FOR SUSPENSION	ORAL	19940928	N/A	NDA	NDA050693	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	1 g/1	10 PACKET in 1 BOX (0069-3051-07) / 1 POWDER, FOR SUSPENSION in 1 PACKET (0069-3051-01)
0069-3051-75	0069-3051	HUMAN PRESCRIPTION DRUG	ZITHROMAX	AZITHROMYCIN DIHYDRATE	POWDER, FOR SUSPENSION	ORAL	19940928	N/A	NDA	NDA050693	Pfizer Laboratories Div Pfizer Inc	AZITHROMYCIN DIHYDRATE	1 g/1	3 PACKET in 1 BOX (0069-3051-75) / 1 POWDER, FOR SUSPENSION in 1 PACKET (0069-3051-01)
59762-3051-1	59762-3051	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	POWDER, FOR SUSPENSION	ORAL	19990212	N/A	NDA AUTHORIZED GENERIC	NDA050693	Greenstone LLC	AZITHROMYCIN DIHYDRATE	1 g/1	10 PACKET in 1 BOX (59762-3051-1) / 1 POWDER, FOR SUSPENSION in 1 PACKET (59762-3051-5)
59762-3051-2	59762-3051	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	POWDER, FOR SUSPENSION	ORAL	19990212	N/A	NDA AUTHORIZED GENERIC	NDA050693	Greenstone LLC	AZITHROMYCIN DIHYDRATE	1 g/1	3 PACKET in 1 BOX (59762-3051-2) / 1 POWDER, FOR SUSPENSION in 1 PACKET (59762-3051-5)