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
63187-065-15	63187-065	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (63187-065-15)
63187-065-20	63187-065	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63187-065-20)
63187-065-30	63187-065	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-065-30)
63187-065-60	63187-065	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-065-60)
63187-065-90	63187-065	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20140401	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-065-90)
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)