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
64980-727-03	64980-727	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209045	Rising Pharma Holdings, Inc.	AZITHROMYCIN DIHYDRATE	250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (64980-727-03)
64980-727-16	64980-727	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209045	Rising Pharma Holdings, Inc.	AZITHROMYCIN DIHYDRATE	250 mg/1	6 TABLET, FILM COATED in 1 BLISTER PACK (64980-727-16)
0527-2370-20	0527-2370	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20241022	N/A	ANDA	ANDA209045	Lannett Company, Inc.	AZITHROMYCIN DIHYDRATE	250 mg/1	6 TABLET, FILM COATED in 1 BLISTER PACK (0527-2370-20)
0527-2370-32	0527-2370	HUMAN PRESCRIPTION DRUG	azithromycin	AZITHROMYCIN	TABLET, FILM COATED	ORAL	20190704	N/A	ANDA	ANDA209045	Lannett Company, Inc.	AZITHROMYCIN DIHYDRATE	250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0527-2370-32)