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
85766-006-05	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (85766-006-05)
85766-006-06	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (85766-006-06)
85766-006-10	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (85766-006-10)
85766-006-24	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20251001	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	24 TABLET, FILM COATED in 1 BOTTLE (85766-006-24)
85766-006-30	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85766-006-30)
85766-006-60	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85766-006-60)
85766-006-90	85766-006	HUMAN PRESCRIPTION DRUG	Ondansetron Hydrochloride	Ondansetron Hydrochloride	TABLET, FILM COATED	ORAL	20250619	N/A	ANDA	ANDA078539	Sportpharm LLC	ONDANSETRON HYDROCHLORIDE	4 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85766-006-90)