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
16714-049-01	16714-049	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200511	N/A	ANDA	ANDA213368	Northstar Rx LLC	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01)
16714-048-01	16714-048	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200511	N/A	ANDA	ANDA213368	Northstar Rx LLC	CHLORPROMAZINE HYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-048-01)
70710-1131-1	70710-1131	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Pharmaceuticals (USA) Inc.	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1)
70710-1131-4	70710-1131	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Pharmaceuticals (USA) Inc.	CHLORPROMAZINE HYDROCHLORIDE	50 mg/1	10 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2)
70771-1509-1	70771-1509	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1)
70771-1509-4	70771-1509	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	100 mg/1	10 BLISTER PACK in 1 CARTON (70771-1509-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)