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
70518-4312-0	70518-4312	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg	TABLET, FILM COATED	ORAL	20250318	N/A	ANDA	ANDA208682	REMEDYREPACK INC.	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	400 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0)
72205-001-31	72205-001	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA208682	Novadoz Pharmaceuticals LLC	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	400 mg/1	50 BLISTER PACK in 1 CARTON (72205-001-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-001-11)
72205-001-30	72205-001	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA208682	Novadoz Pharmaceuticals LLC	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72205-001-30)
72205-001-05	72205-001	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA208682	Novadoz Pharmaceuticals LLC	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72205-001-05)
72789-080-10	72789-080	HUMAN PRESCRIPTION DRUG	Moxifloxacin Hydrochloride Tablets, 400 mg	Moxifloxacin Hydrochloride Tablets, 400 mg	TABLET, FILM COATED	ORAL	20200410	N/A	ANDA	ANDA208682	PD-Rx Pharmaceuticals, Inc.	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	400 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-080-10)