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
72789-037-10	72789-037	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20200217	N/A	ANDA	ANDA202632	PD-Rx Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-037-10)
72789-038-10	72789-038	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20191210	N/A	ANDA	ANDA202632	PD-Rx Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-038-10)
0904-7407-04	0904-7407	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20240308	N/A	ANDA	ANDA202632	Major Pharmaceuticals	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 BLISTER PACK in 1 CARTON (0904-7407-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7407-06	0904-7407	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20240308	N/A	ANDA	ANDA202632	Major Pharmaceuticals	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	50 BLISTER PACK in 1 CARTON (0904-7407-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
71335-2329-1	71335-2329	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20240502	N/A	ANDA	ANDA202632	Bryant Ranch Prepack	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-2329-1)
71335-2329-2	71335-2329	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20240103	N/A	ANDA	ANDA202632	Bryant Ranch Prepack	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2329-2)
68084-722-65	68084-722	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20140319	N/A	ANDA	ANDA202632	American Health Packaging	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11)
72789-350-10	72789-350	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230915	N/A	ANDA	ANDA202632	PD-Rx Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-350-10)
50090-6595-1	50090-6595	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230818	N/A	ANDA	ANDA202632	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6595-1)
50090-6609-0	50090-6609	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230823	N/A	ANDA	ANDA202632	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-6609-0)
50090-6609-1	50090-6609	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20231031	N/A	ANDA	ANDA202632	A-S Medication Solutions	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)
65862-603-30	65862-603	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20140304	N/A	ANDA	ANDA202632	Aurobindo Pharma Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-603-30)
65862-603-55	65862-603	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20140304	N/A	ANDA	ANDA202632	Aurobindo Pharma Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (65862-603-55) / 1 TABLET, FILM COATED in 1 BLISTER PACK (65862-603-10)
65862-603-99	65862-603	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20140304	N/A	ANDA	ANDA202632	Aurobindo Pharma Limited	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-603-99)
57237-156-30	57237-156	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20140304	N/A	ANDA	ANDA202632	Rising Pharma Holdings, Inc.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30)
50268-576-13	50268-576	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride	Moxifloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20160722	N/A	ANDA	ANDA202632	AvPAK	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11)
70518-3738-0	70518-3738	HUMAN PRESCRIPTION DRUG	MOXIFLOXACIN HYDROCHLORIDE	moxifloxacin hydrochloride	TABLET, FILM COATED	ORAL	20230530	N/A	ANDA	ANDA202632	REMEDYREPACK INC.	MOXIFLOXACIN HYDROCHLORIDE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3738-0)