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
51407-838-05	51407-838	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240203	N/A	ANDA	ANDA208058	Golden State Medical Supply, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51407-838-05)
23155-890-03	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	30 TABLET, FILM COATED in 1 BOTTLE (23155-890-03)
23155-890-05	23155-890	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	80 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (23155-890-05)
23155-890-09	23155-890	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	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (23155-890-09)
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)
51407-836-05	51407-836	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240203	N/A	ANDA	ANDA208058	Golden State Medical Supply, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (51407-836-05)