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
71335-0205-6	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	4 TABLET, FILM COATED in 1 BOTTLE (71335-0205-6)
71335-0205-7	71335-0205	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180216	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0205-7)
71335-0205-8	71335-0205	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180301	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71335-0205-8)
71335-0205-9	71335-0205	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20180403	N/A	ANDA	ANDA078539	Bryant Ranch Prepack	ONDANSETRON HYDROCHLORIDE	4 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0205-9)