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
68462-105-30	68462-105	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077535	Glenmark Pharmaceuticals Inc., USA	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-105-30)
68462-105-33	68462-105	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077535	Glenmark Pharmaceuticals Inc., USA	ONDANSETRON HYDROCHLORIDE	4 mg/1	1 BLISTER PACK in 1 CARTON (68462-105-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
68462-106-30	68462-106	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077535	Glenmark Pharmaceuticals Inc., USA	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-106-30)
68462-106-33	68462-106	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077535	Glenmark Pharmaceuticals Inc., USA	ONDANSETRON HYDROCHLORIDE	8 mg/1	1 BLISTER PACK in 1 CARTON (68462-106-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
43063-770-06	43063-770	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET, FILM COATED	ORAL	20140303	N/A	ANDA	ANDA077535	PD-Rx Pharmaceuticals, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-770-06)