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
50090-4100-0	50090-4100	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET	ORAL	20190125	N/A	ANDA	ANDA205348	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET in 1 BOTTLE (50090-4100-0)
50090-4058-1	50090-4058	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET	ORAL	20190115	N/A	ANDA	ANDA205348	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET in 1 BOTTLE (50090-4058-1)
51991-943-33	51991-943	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET	ORAL	20170502	20250731	ANDA	ANDA205348	Breckenridge Pharmaceutical, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET in 1 BOTTLE (51991-943-33)