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
70518-4588-0	70518-4588	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20260320	N/A	ANDA	ANDA077851	REMEDYREPACK INC.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET in 1 BLISTER PACK (70518-4588-0)
69339-172-01	69339-172	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20250627	N/A	ANDA	ANDA077851	Natco Pharma USA LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	100 TABLET in 1 BOTTLE (69339-172-01)
69339-172-03	69339-172	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20221024	N/A	ANDA	ANDA077851	Natco Pharma USA LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (69339-172-03)
69339-172-05	69339-172	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20250627	N/A	ANDA	ANDA077851	Natco Pharma USA LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	500 TABLET in 1 BOTTLE (69339-172-05)
71335-0132-0	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0132-0)
71335-0132-1	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-0132-1)
71335-0132-2	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)
71335-0132-3	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0132-3)
71335-0132-4	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0132-4)
71335-0132-5	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-0132-5)
71335-0132-6	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71335-0132-6)
63304-459-30	63304-459	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077851	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-459-30)
71335-0132-7	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0132-7)
71335-0132-8	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71335-0132-8)
71335-0132-9	71335-0132	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140403	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0132-9)
63187-236-10	63187-236	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63187-236-10)
63187-236-15	63187-236	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (63187-236-15)
63187-236-20	63187-236	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63187-236-20)
63304-458-30	63304-458	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077851	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-458-30)
71335-0815-0	71335-0815	HUMAN PRESCRIPTION DRUG	ondansetron	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20120824	N/A	ANDA	ANDA077851	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	8 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (71335-0815-0)