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
16714-048-01	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)
70771-1506-1	70771-1506	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1506-1)
70771-1506-4	70771-1506	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (70771-1506-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1506-2)
70771-1510-1	70771-1510	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1510-1)
70771-1510-4	70771-1510	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	N/A	ANDA	ANDA213368	Zydus Lifesciences Limited	CHLORPROMAZINE HYDROCHLORIDE	200 mg/1	10 BLISTER PACK in 1 CARTON (70771-1510-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1510-2)
0904-7132-61	0904-7132	HUMAN PRESCRIPTION DRUG	Chlorpromazine hydrochloride	Chlorpromazine hydrochloride	TABLET, FILM COATED	ORAL	20200127	20260630	ANDA	ANDA213368	Major Pharmaceuticals	CHLORPROMAZINE HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 CARTON (0904-7132-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK