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
68788-9368-1	68788-9368	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20120612	N/A	ANDA	ANDA078539	Preferred Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1)
68788-9368-2	68788-9368	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20170623	N/A	ANDA	ANDA078539	Preferred Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (68788-9368-2)
68788-9368-3	68788-9368	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20120612	N/A	ANDA	ANDA078539	Preferred Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-9368-3)
83008-074-20	83008-074	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20240725	20280131	ANDA	ANDA078539	Quality Care Products, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (83008-074-20)
83008-074-30	83008-074	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20240725	20280131	ANDA	ANDA078539	Quality Care Products, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (83008-074-30)
50268-621-15	50268-621	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20160805	N/A	ANDA	ANDA078539	AvPAK	ONDANSETRON HYDROCHLORIDE	4 mg/1	50 BLISTER PACK in 1 BOX (50268-621-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-621-11)
70518-1585-0	70518-1585	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20181024	N/A	ANDA	ANDA078539	REMEDYREPACK INC.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-0)
70518-1585-6	70518-1585	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20251001	N/A	ANDA	ANDA078539	REMEDYREPACK INC.	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-6)
51655-933-04	51655-933	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20221025	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04)
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)
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
57237-076-30	57237-076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Rising Pharma Holdings, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (57237-076-30)
57237-076-50	57237-076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20221004	N/A	ANDA	ANDA078539	Rising Pharma Holdings, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57237-076-50)
50090-6342-0	50090-6342	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-6342-0)
50090-6342-1	50090-6342	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (50090-6342-1)
50090-6342-2	50090-6342	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-6342-2)
50090-6342-4	50090-6342	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (50090-6342-4)
50090-6342-5	50090-6342	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230123	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (50090-6342-5)
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)
76420-916-00	76420-916	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250128	N/A	ANDA	ANDA078539	Asclemed USA, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76420-916-00)