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
82804-034-30	82804-034	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20231101	N/A	ANDA	ANDA212091	Proficient Rx LP	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-034-30)
82804-034-60	82804-034	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20231101	N/A	ANDA	ANDA212091	Proficient Rx LP	LURASIDONE HYDROCHLORIDE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-034-60)
82804-034-90	82804-034	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20231101	N/A	ANDA	ANDA212091	Proficient Rx LP	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-034-90)
50090-7078-0	50090-7078	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20240131	N/A	ANDA	ANDA212091	A-S Medication Solutions	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7078-0)
70436-093-01	70436-093	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70436-093-01)
70436-093-04	70436-093	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-093-04)
70436-094-01	70436-094	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70436-094-01)
70436-094-04	70436-094	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-094-04)
70436-095-01	70436-095	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70436-095-01)
70436-095-04	70436-095	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-095-04)
70436-096-01	70436-096	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70436-096-01)
70436-096-04	70436-096	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-096-04)
70436-097-01	70436-097	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70436-097-01)
70436-097-04	70436-097	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212091	Slate Run Pharmaceuticals, LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-097-04)