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
63304-459-30	63304-459	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077851	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-459-30)
51407-004-05	51407-004	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20250107	N/A	ANDA	ANDA077851	Golden State Medical Supply, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	500 TABLET in 1 BOTTLE (51407-004-05)
51407-004-30	51407-004	HUMAN PRESCRIPTION DRUG	Ondansetron	Ondansetron	TABLET	ORAL	20250108	N/A	ANDA	ANDA077851	Golden State Medical Supply, Inc.	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (51407-004-30)
63304-458-30	63304-458	HUMAN PRESCRIPTION DRUG	ONDANSETRON	ONDANSETRON	TABLET, FILM COATED	ORAL	20070625	N/A	ANDA	ANDA077851	Sun Pharmaceutical Industries, Inc.	ONDANSETRON HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-458-30)
63187-513-10	63187-513	HUMAN PRESCRIPTION DRUG	ondansetron	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63187-513-10)
63187-513-15	63187-513	HUMAN PRESCRIPTION DRUG	ondansetron	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (63187-513-15)
63187-513-20	63187-513	HUMAN PRESCRIPTION DRUG	ondansetron	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63187-513-20)
63187-513-30	63187-513	HUMAN PRESCRIPTION DRUG	ondansetron	ondansetron hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA077851	Proficient Rx LP	ONDANSETRON HYDROCHLORIDE	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-513-30)