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
76420-411-30	76420-411	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	ASCLEMED USA INC.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-411-30)
76420-411-60	76420-411	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	ASCLEMED USA INC.	ONDANSETRON HYDROCHLORIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-411-60)
76420-411-90	76420-411	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	ASCLEMED USA INC.	ONDANSETRON HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-411-90)
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)
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)
72162-2365-5	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)
55700-631-10	55700-631	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180525	20270531	ANDA	ANDA078539	Quality Care Products LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (55700-631-10)
55700-631-20	55700-631	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180525	20270531	ANDA	ANDA078539	Quality Care Products LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (55700-631-20)
55700-631-30	55700-631	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180525	20280131	ANDA	ANDA078539	Quality Care Products LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55700-631-30)
80425-0075-3	80425-0075	HUMAN PRESCRIPTION DRUG	Ondansetron HCL	Ondansetron HCL	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Advanced Rx of Tennessee, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (80425-0075-3)
80425-0075-4	80425-0075	HUMAN PRESCRIPTION DRUG	Ondansetron HCL	Ondansetron HCL	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Advanced Rx of Tennessee, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0075-4)
80425-0075-5	80425-0075	HUMAN PRESCRIPTION DRUG	Ondansetron HCL	Ondansetron HCL	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	Advanced Rx of Tennessee, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0075-5)
60760-636-10	60760-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20070731	N/A	ANDA	ANDA078539	St. Mary's Medical Park Pharmacy	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-10)
60760-636-16	60760-636	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230303	N/A	ANDA	ANDA078539	St. Mary's Medical Park Pharmacy	ONDANSETRON HYDROCHLORIDE	4 mg/1	16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-16)