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
68071-2053-2	68071-2053	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250114	N/A	ANDA	ANDA078539	NuCare Pharmaceuticals,Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-2053-2)
65862-187-03	65862-187	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Aurobindo Pharma Limited	ONDANSETRON HYDROCHLORIDE	4 mg/1	1 BLISTER PACK in 1 CARTON (65862-187-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
65862-187-05	65862-187	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Aurobindo Pharma Limited	ONDANSETRON HYDROCHLORIDE	4 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-187-05)
65862-187-10	65862-187	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Aurobindo Pharma Limited	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 BLISTER PACK in 1 CARTON (65862-187-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-187-30	65862-187	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Aurobindo Pharma Limited	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)
65862-187-99	65862-187	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Aurobindo Pharma Limited	ONDANSETRON HYDROCHLORIDE	4 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-187-99)
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)
85509-1076-1	85509-1076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078539	PHOENIX RX LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (85509-1076-1)
85509-1076-2	85509-1076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078539	PHOENIX RX LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (85509-1076-2)
85509-1076-3	85509-1076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078539	PHOENIX RX LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85509-1076-3)
85509-1076-5	85509-1076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078539	PHOENIX RX LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (85509-1076-5)
85509-1076-6	85509-1076	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078539	PHOENIX RX LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85509-1076-6)
85509-1057-4	85509-1057	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA078539	PHOENIX RX LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (85509-1057-4)
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)