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
67046-1637-3	67046-1637	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20251231	N/A	ANDA	ANDA213248	Coupler LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1637-3)
62332-498-10	62332-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	100 BLISTER PACK in 1 CARTON (62332-498-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
67046-1659-3	67046-1659	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20260212	N/A	ANDA	ANDA213248	Coupler LLC	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1659-3)
62332-498-30	62332-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-498-30)
62332-498-71	62332-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-498-71)
62332-498-90	62332-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-498-90)
62332-498-91	62332-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-498-91)
62332-494-10	62332-494	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	100 BLISTER PACK in 1 CARTON (62332-494-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
62332-494-30	62332-494	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-494-30)
62332-494-71	62332-494	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62332-494-71)
62332-494-90	62332-494	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-494-90)
62332-494-91	62332-494	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-494-91)