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
50090-3147-1	50090-3147	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20171002	N/A	ANDA	ANDA076938	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-3147-1)
50090-3147-0	50090-3147	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20190425	N/A	ANDA	ANDA076938	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-3147-0)
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)
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)
0904-6406-04	0904-6406	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA076938	Major Pharmaceuticals	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 BLISTER PACK in 1 CARTON (0904-6406-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-6406-06	0904-6406	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20140305	N/A	ANDA	ANDA076938	Major Pharmaceuticals	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	50 BLISTER PACK in 1 CARTON (0904-6406-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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)
70518-3713-0	70518-3713	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20230412	N/A	ANDA	ANDA076938	REMEDYREPACK INC.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3713-0)
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)
53002-2723-1	53002-2723	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20220401	N/A	ANDA	ANDA076938	RPK Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (53002-2723-1)
53002-2723-7	53002-2723	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20220401	N/A	ANDA	ANDA076938	RPK Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (53002-2723-7)
50090-5833-0	50090-5833	HUMAN PRESCRIPTION DRUG	Moxifloxacin	Moxifloxacin	TABLET, FILM COATED	ORAL	20211027	N/A	ANDA	ANDA076938	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-5833-0)