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
63187-636-01	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (63187-636-01)
63187-636-03	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20170501	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (63187-636-03)
63187-636-06	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (63187-636-06)
63187-636-10	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20160502	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 BLISTER PACK in 1 CARTON (63187-636-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
63187-636-12	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180904	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (63187-636-12)
63187-636-15	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20160502	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (63187-636-15)
63187-636-20	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20160502	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63187-636-20)
63187-636-30	63187-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20160502	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-636-30)
16714-159-01	16714-159	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20210406	N/A	ANDA	ANDA078539	NorthStar Rx LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-159-01)
72162-2365-5	72162-2365	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	8 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-2365-5)
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)
50268-622-15	50268-622	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20160805	N/A	ANDA	ANDA078539	AvPAK	ONDANSETRON HYDROCHLORIDE	8 mg/1	50 BLISTER PACK in 1 BOX (50268-622-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-622-11)
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)
51655-933-43	51655-933	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220720	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43)
51655-933-53	51655-933	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220916	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-53)
51655-933-54	51655-933	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230511	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-54)
51655-933-55	51655-933	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230509	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-55)
51655-933-87	51655-933	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220720	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87)
72162-2364-5	72162-2364	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-2364-5)
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)