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
0832-6021-00	0832-6021	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20210806	N/A	ANDA	ANDA084115	Upsher-Smith Laboratories, LLC	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0832-6021-00)
0832-6021-01	0832-6021	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20210806	N/A	ANDA	ANDA084115	Upsher-Smith Laboratories, LLC	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	1 BLISTER PACK in 1 CARTON (0832-6021-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6021-89)
0832-6021-10	0832-6021	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20210806	N/A	ANDA	ANDA084115	Upsher-Smith Laboratories, LLC	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0832-6021-10)
70518-4295-0	70518-4295	HUMAN PRESCRIPTION DRUG	Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	TABLET, FILM COATED	ORAL	20250226	N/A	ANDA	ANDA084115	REMEDYREPACK INC.	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	100 POUCH in 1 BOX (70518-4295-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4295-1)