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
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)
16714-160-01	16714-160	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20210406	N/A	ANDA	ANDA078539	NorthStar Rx LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16714-160-01)
51655-016-27	51655-016	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220916	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-27)
51655-016-53	51655-016	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220916	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53)
51655-016-54	51655-016	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220808	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-54)
51655-016-87	51655-016	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220921	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87)
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
54348-819-02	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 (54348-819-02) / 2 TABLET, FILM COATED in 1 BOTTLE
54348-819-04	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 (54348-819-04) / 4 TABLET, FILM COATED in 1 BOTTLE
50090-3185-0	50090-3185	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180117	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	8 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (50090-3185-0)
50090-3185-1	50090-3185	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-1)
50090-3185-2	50090-3185	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	8 mg/1	3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-2)
50090-3185-3	50090-3185	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-3)
50090-3185-4	50090-3185	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA078539	A-S Medication Solutions	ONDANSETRON HYDROCHLORIDE	8 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-4)
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)
71610-119-88	71610-119	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA078539	Aphena Pharma Solutions - Tennessee, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	900 TABLET, FILM COATED in 1 BOTTLE (71610-119-88)
68071-3801-1	68071-3801	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20250224	N/A	ANDA	ANDA078539	NuCare Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-3801-1)
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)
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)
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)