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
63629-8357-1	63629-8357	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA076938	Bryant Ranch Prepack	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1)
63629-8357-2	63629-8357	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20201105	N/A	ANDA	ANDA076938	Bryant Ranch Prepack	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2)
55111-112-01	55111-112	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA076938	Dr. Reddy's Laboratories Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01)
55111-112-05	55111-112	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA076938	Dr. Reddy's Laboratories Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05)
55111-112-30	55111-112	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA076938	Dr. Reddy's Laboratories Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55111-112-30)
55111-112-66	55111-112	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA076938	Dr. Reddy's Laboratories Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	5 BLISTER PACK in 1 CARTON (55111-112-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)
72789-233-10	72789-233	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20220215	N/A	ANDA	ANDA076938	PD-Rx Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)