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
0832-6019-10	0832-6019	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20210806	N/A	ANDA	ANDA084113	Upsher-Smith Laboratories, LLC	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10)
0832-6019-01	0832-6019	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20210806	N/A	ANDA	ANDA084113	Upsher-Smith Laboratories, LLC	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	1 BLISTER PACK in 1 CARTON (0832-6019-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89)
0832-6019-00	0832-6019	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20210806	N/A	ANDA	ANDA084113	Upsher-Smith Laboratories, LLC	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00)
70518-3674-0	70518-3674	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA084113	REMEDYREPACK INC.	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	100 POUCH in 1 BOX (70518-3674-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3674-1)
70518-3674-2	70518-3674	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20231204	N/A	ANDA	ANDA084113	REMEDYREPACK INC.	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3674-2)