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
51655-415-54	51655-415	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20171228	N/A	ANDA	ANDA078539	Northwind Pharmaceuticals, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (51655-415-54)
51655-415-55	51655-415	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA078539	Northwind Pharmaceuticals, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (51655-415-55)
51655-415-87	51655-415	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20181024	N/A	ANDA	ANDA078539	Northwind Pharmaceuticals, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (51655-415-87)
85766-006-90	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm, Inc. dba Sportpharm	ONDANSETRON HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85766-006-90)
68071-4705-4	68071-4705	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20190111	N/A	ANDA	ANDA078539	NuCare Pharmaceuticals,Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (68071-4705-4)
71335-1855-0	71335-1855	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1855-0)
71335-1855-1	71335-1855	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1855-1)
71335-1855-2	71335-1855	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (71335-1855-2)
71335-1855-3	71335-1855	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1855-3)
68071-5047-3	68071-5047	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA078539	NuCare Pharmaceuticals,Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-5047-3)
42708-044-05	42708-044	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA078539	QPharma Inc	ONDANSETRON HYDROCHLORIDE	4 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (42708-044-05)
54348-819-00	54348-819	HUMAN PRESCRIPTION DRUG	Ondansetron	ONDANSETRON	TABLET, FILM COATED	ORAL	20190710	N/A	ANDA	ANDA078539	PharmPak, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	1 BOTTLE in 1 BOX (54348-819-00) / 1 TABLET, FILM COATED in 1 BOTTLE
67296-0902-1	67296-0902	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	RedPharm Drug, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (67296-0902-1)
67296-0902-2	67296-0902	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20210101	N/A	ANDA	ANDA078539	RedPharm Drug, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (67296-0902-2)
67296-0902-3	67296-0902	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	RedPharm Drug, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-0902-3)
70518-4245-0	70518-4245	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA078539	REMEDYREPACK INC.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4245-0)
72789-034-12	72789-034	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20191202	N/A	ANDA	ANDA078539	PD-Rx Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)
76420-917-01	76420-917	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250128	N/A	ANDA	ANDA078539	Asclemed USA, Inc.	ONDANSETRON HYDROCHLORIDE	24 mg/1	1 BLISTER PACK in 1 CARTON (76420-917-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK
51655-813-54	51655-813	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20210610	N/A	ANDA	ANDA078539	Northwind Pharmaceuticals, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-813-54)
42708-059-05	42708-059	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180419	N/A	ANDA	ANDA078539	QPharma, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05)