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
23155-804-01	23155-804	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, COATED	ORAL	20230625	N/A	ANDA	ANDA213590	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	CHLORPROMAZINE HYDROCHLORIDE	25 mg/1	100 TABLET, COATED in 1 BOTTLE (23155-804-01)
23155-806-01	23155-806	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, COATED	ORAL	20230625	N/A	ANDA	ANDA213590	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	CHLORPROMAZINE HYDROCHLORIDE	100 mg/1	100 TABLET, COATED in 1 BOTTLE (23155-806-01)
23155-805-01	23155-805	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, COATED	ORAL	20230625	N/A	ANDA	ANDA213590	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	100 TABLET, COATED in 1 BOTTLE (23155-805-01)
23155-803-01	23155-803	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, COATED	ORAL	20230625	N/A	ANDA	ANDA213590	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	CHLORPROMAZINE HYDROCHLORIDE	10 mg/1	100 TABLET, COATED in 1 BOTTLE (23155-803-01)
23155-807-01	23155-807	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, COATED	ORAL	20230625	N/A	ANDA	ANDA213590	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	100 TABLET, COATED in 1 BOTTLE (23155-807-01)