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
63402-312-04	63402-312	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20120426	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	4 BLISTER PACK in 1 CARTON (63402-312-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-312-07)
63402-312-10	63402-312	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20120426	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	10 BLISTER PACK in 1 CARTON (63402-312-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-312-01)
63402-312-30	63402-312	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20120426	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63402-312-30)
63402-312-50	63402-312	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20120426	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63402-312-50)
63402-312-90	63402-312	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20120426	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63402-312-90)