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
23155-890-18	23155-890	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20231019	N/A	ANDA	ANDA208058	Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30000 TABLET, FILM COATED in 1 CONTAINER (23155-890-18)
23155-891-01	23155-891	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20250820	N/A	ANDA	ANDA208058	Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (23155-891-01)
23155-891-03	23155-891	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20250820	N/A	ANDA	ANDA208058	Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (23155-891-03)
23155-891-05	23155-891	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20250820	N/A	ANDA	ANDA208058	Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (23155-891-05)
23155-891-10	23155-891	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20250820	N/A	ANDA	ANDA208058	Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (23155-891-10)
23155-891-18	23155-891	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20231019	N/A	ANDA	ANDA208058	Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	20000 TABLET, FILM COATED in 1 CONTAINER (23155-891-18)