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
71335-0815-4	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	3 TABLET, FILM COATED in 1 BOTTLE (71335-0815-4)
71335-0815-5	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	12 TABLET, FILM COATED in 1 BOTTLE (71335-0815-5)
71335-0815-6	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	20 TABLET, FILM COATED in 1 BOTTLE (71335-0815-6)
71335-0815-7	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	30 TABLET, FILM COATED in 1 BOTTLE (71335-0815-7)
71335-0815-8	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	60 TABLET, FILM COATED in 1 BOTTLE (71335-0815-8)
71335-0815-9	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	6 TABLET, FILM COATED in 1 BOTTLE (71335-0815-9)
69339-172-05	69339-172	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20221024	N/A	ANDA	ANDA077851	Natco Pharma USA LLC	ONDANSETRON HYDROCHLORIDE	8 mg/1	500 TABLET in 1 BOTTLE (69339-172-05)