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
46708-497-10	46708-497	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	100 BLISTER PACK in 1 CARTON (46708-497-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
46708-497-30	46708-497	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-497-30)
46708-497-71	46708-497	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-497-71)
46708-497-90	46708-497	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-497-90)
46708-497-91	46708-497	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-497-91)
46708-498-10	46708-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	100 BLISTER PACK in 1 CARTON (46708-498-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
46708-498-30	46708-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-498-30)
46708-498-71	46708-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-498-71)
46708-498-90	46708-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-498-90)
46708-498-91	46708-498	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230124	N/A	ANDA	ANDA213248	Alembic Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-498-91)
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)