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
62756-131-02	62756-131	HUMAN PRESCRIPTION DRUG	ondansetron hydrochloride	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077050	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 BLISTER PACK in 1 DOSE PACK (62756-131-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK
62756-131-01	62756-131	HUMAN PRESCRIPTION DRUG	ondansetron hydrochloride	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077050	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-131-01)
62756-130-02	62756-130	HUMAN PRESCRIPTION DRUG	ondansetron hydrochloride	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077050	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	10 BLISTER PACK in 1 DOSE PACK (62756-130-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK
62756-130-01	62756-130	HUMAN PRESCRIPTION DRUG	ondansetron hydrochloride	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077050	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-130-01)