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
63402-302-90	63402-302	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20111207	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63402-302-90)
63402-302-04	63402-302	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20111207	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	4 BLISTER PACK in 1 CARTON (63402-302-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-07)
63402-302-10	63402-302	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20111207	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (63402-302-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-01)
63402-302-30	63402-302	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20111207	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63402-302-30)
63402-302-50	63402-302	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20111207	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63402-302-50)
63402-304-04	63402-304	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	4 BLISTER PACK in 1 CARTON (63402-304-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-07)
63402-304-10	63402-304	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	10 BLISTER PACK in 1 CARTON (63402-304-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-01)
63402-304-30	63402-304	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63402-304-30)
63402-304-50	63402-304	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63402-304-50)
63402-304-90	63402-304	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63402-304-90)
63402-306-04	63402-306	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20130712	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	4 BLISTER PACK in 1 CARTON (63402-306-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-306-07)
63402-306-10	63402-306	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20130712	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	10 BLISTER PACK in 1 CARTON (63402-306-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-306-01)
63402-306-30	63402-306	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20130712	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63402-306-30)
63402-306-50	63402-306	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20130712	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63402-306-50)
63402-306-90	63402-306	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20130712	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63402-306-90)
63402-308-04	63402-308	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	4 BLISTER PACK in 1 CARTON (63402-308-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-308-07)
63402-308-10	63402-308	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	10 BLISTER PACK in 1 CARTON (63402-308-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-308-01)
63402-308-30	63402-308	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63402-308-30)
63402-308-50	63402-308	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63402-308-50)
63402-308-90	63402-308	HUMAN PRESCRIPTION DRUG	Latuda	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20101028	N/A	NDA	NDA200603	Sumitomo Pharma America, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63402-308-90)