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
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)
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)
43063-792-06	43063-792	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20171006	N/A	ANDA	ANDA078539	PD-Rx Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)
51655-813-54	51655-813	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20210610	N/A	ANDA	ANDA078539	Northwind Health Company, LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-813-54)
71205-744-10	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230116	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-744-10)
71205-744-30	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230116	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-744-30)
71205-744-60	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230116	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-744-60)
71205-744-90	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230116	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-744-90)
71205-744-12	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230613	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71205-744-12)
71205-744-15	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230116	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71205-744-15)
71205-744-20	71205-744	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20230116	N/A	ANDA	ANDA078539	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-744-20)
70518-3511-0	70518-3511	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20220906	N/A	ANDA	ANDA078539	REMEDYREPACK INC.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-0)
70518-3511-1	70518-3511	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250702	N/A	ANDA	ANDA078539	REMEDYREPACK INC.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-1)
71335-0205-2	71335-0205	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (71335-0205-2)
71335-0205-4	71335-0205	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180214	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0205-4)
71335-0205-5	71335-0205	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180321	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-0205-5)